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FDA 510(k)

VITA-MIST AIR COMPRESSOR & NEBULIZER

K-Number: K832072 · 1983-09-12

ApplicantVita Medics
Decision Date1983-09-12
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITA-MIST AIR COMPRESSOR & NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Vita Medics. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832072. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA-MIST AIR COMPRESSOR & NEBULIZER?

VITA-MIST AIR COMPRESSOR & NEBULIZER is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Vita Medics. The 510(k) number is K832072.

When did VITA-MIST AIR COMPRESSOR & NEBULIZER receive FDA 510(k) clearance?

VITA-MIST AIR COMPRESSOR & NEBULIZER received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832072.

Who is the listed applicant for VITA-MIST AIR COMPRESSOR & NEBULIZER?

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

What is the FDA product code for VITA-MIST AIR COMPRESSOR & NEBULIZER?

The FDA product code for VITA-MIST AIR COMPRESSOR & NEBULIZER is BTI.

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Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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