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FDA 510(k)

BNOS MICROVENT(TM), MODEL AC AND MODEL AO

K-Number: K930533 · 1993-03-29

ApplicantBnos Meditech, Ltd.
Decision Date1993-03-29
Product CodeBZT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BNOS MICROVENT(TM), MODEL AC AND MODEL AO is the device name listed in this FDA 510(k) record. The listed applicant is Bnos Meditech, Ltd.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K930533. The device is classified under product code BZT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BNOS MICROVENT(TM), MODEL AC AND MODEL AO?

BNOS MICROVENT(TM), MODEL AC AND MODEL AO is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Bnos Meditech, Ltd.. The 510(k) number is K930533.

When did BNOS MICROVENT(TM), MODEL AC AND MODEL AO receive FDA 510(k) clearance?

BNOS MICROVENT(TM), MODEL AC AND MODEL AO received FDA 510(k) clearance on 1993-03-29, under 510(k) number K930533.

Who is the listed applicant for BNOS MICROVENT(TM), MODEL AC AND MODEL AO?

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

What is the FDA product code for BNOS MICROVENT(TM), MODEL AC AND MODEL AO?

The FDA product code for BNOS MICROVENT(TM), MODEL AC AND MODEL AO is BZT.

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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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