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FDA 510(k)

RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM

K-Number: K895849 · 1989-12-22

ApplicantRespironics, Inc.
Decision Date1989-12-22
Product CodeBYT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1989-12-22 under 510(k) number K895849. The device is classified under product code BYT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM?

RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Respironics, Inc.. The 510(k) number is K895849.

When did RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM receive FDA 510(k) clearance?

RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM received FDA 510(k) clearance on 1989-12-22, under 510(k) number K895849.

Who is the listed applicant for RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM?

The FDA 510(k) record lists Respironics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM?

The FDA product code for RESPIRONICS VACUVEST RESPIRATORY SUPPORT SYSTEM is BYT.

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Related Devices (Code: BYT)

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.

K082657RTX RESPIRATORMedivent LimitedK072290PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUSDima Italia SrlK924341HAYEK OSCILLATOR(TM)Respironics, Inc.K910947NEV-10 NEGATIVE PRESSURE VENTILATORLifecare Services, Inc.K905530PURITAN-BENNETT COMPANION 500 LIQUID OXYGEN SYSTEMPuritan Bennett Corp.K902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMJ. H. Emerson 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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