Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE

K-Number: K951127 · 1995-03-24

ApplicantHewlett-Packard GmbH
Decision Date1995-03-24
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard GmbH. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K951127. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE?

HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is Hewlett-Packard GmbH. The 510(k) number is K951127.

When did HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE receive FDA 510(k) clearance?

HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE received FDA 510(k) clearance on 1995-03-24, under 510(k) number K951127.

Who is the listed applicant for HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE?

The FDA 510(k) record lists Hewlett-Packard GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE?

The FDA product code for HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE is CCK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hewlett-Packard GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K993383HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENT MONITOR MODELS M3000A, M3046A, M3015A, REL.BK992273HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENT MONITOR M3000A/M3046A/M3016A,REL BK992595HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K WITH EASI-ST SEGMENT MEASUREMENT, HP VIRIDIA CMS 24/26, REV K WITHK992674HP VIRIDIA CMS PATIENT MONITOR WITH EEG PARAMETER, MODEL M1027AK990476HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26, MODEL REV. K WITH EASI-ECG OPTIONK991773HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26, HP VIRIDIA MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE P

View all 16 devices →

Related Devices (Code: CCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑