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FDA 510(k)

GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR

K-Number: K902906 · 1990-10-15

ApplicantGas-Vak
Decision Date1990-10-15
Product CodeFLI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Gas-Vak. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K902906. The device is classified under product code FLI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR?

GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Gas-Vak. The 510(k) number is K902906.

When did GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR receive FDA 510(k) clearance?

GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR received FDA 510(k) clearance on 1990-10-15, under 510(k) number K902906.

Who is the listed applicant for GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR?

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

What is the FDA product code for GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR?

The FDA product code for GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR is FLI.

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 Gas-Vak 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.

K890438GAS-VAK(R), MODEL 300

Related Devices (Code: FLI)

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.

K904921STERI-VAC(TM) AERATOR MODEL XL3M Health Care, Ltd.K831595CASTLE MODEL 3341 & 3441 & 4141 GAS AERCastle Co.K830165BEAR JET 150 VENTILATORBear Medical Systems, Inc.K813201CASTLE #3241 GAS AERATORSybron Corp.K790677EO EVACUATING SYSTEM ICastle Co.K781484CASTLE MODEL 3146 GAS AERATORCastle Co.

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.

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