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)

SIEMENS ETCO2 CARTRIDGE

K-Number: K905775 · 1991-03-11

ApplicantSiemens Medical Electronics
Decision Date1991-03-11
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS ETCO2 CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1991-03-11 under 510(k) number K905775. 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 SIEMENS ETCO2 CARTRIDGE?

SIEMENS ETCO2 CARTRIDGE is a medical device that received FDA 510(k) clearance on 1991-03-11. The listed applicant is Siemens Medical Electronics. The 510(k) number is K905775.

When did SIEMENS ETCO2 CARTRIDGE receive FDA 510(k) clearance?

SIEMENS ETCO2 CARTRIDGE received FDA 510(k) clearance on 1991-03-11, under 510(k) number K905775.

Who is the listed applicant for SIEMENS ETCO2 CARTRIDGE?

The FDA 510(k) record lists Siemens Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS ETCO2 CARTRIDGE?

The FDA product code for SIEMENS ETCO2 CARTRIDGE 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 Siemens Medical Electronics 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.

K935043SIEMENS CLINICAL WORK STATIONK921930SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFIK920445SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIESK914765SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYSK912070SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNITK913489SIEMENS MICRO2 PULSE OXIMETER

View all 15 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.

↑