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)

VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM

K-Number: K890058 · 1989-11-21

ApplicantVascular Technology Incorporated
Decision Date1989-11-21
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technology Incorporated. It received FDA 510(k) clearance on 1989-11-21 under 510(k) number K890058. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM?

VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM is a medical device that received FDA 510(k) clearance on 1989-11-21. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K890058.

When did VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM receive FDA 510(k) clearance?

VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM received FDA 510(k) clearance on 1989-11-21, under 510(k) number K890058.

Who is the listed applicant for VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM?

The FDA 510(k) record lists Vascular Technology Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM?

The FDA product code for VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM is CCL.

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 Vascular Technology Incorporated 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.

K082870VTI INTRAOPERATIVE DOPPLER SYSTEMSK031091VTI 20 MHZ GATED DOPPLERK002990VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001K944764VTI DISPOSABLE PRESSURE DISPLAY SETK922738VTI OXYGEN ANALYZERK883960GIPHY MONITOR

View all 11 devices →

Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, 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.

↑