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FDA 510(k)

RESP-BAC BACTERIA FILTER

K-Number: K851070 · 1985-06-14

ApplicantMedicomp, Inc.
Decision Date1985-06-14
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESP-BAC BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medicomp, Inc.. It received FDA 510(k) clearance on 1985-06-14 under 510(k) number K851070. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESP-BAC BACTERIA FILTER?

RESP-BAC BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1985-06-14. The listed applicant is Medicomp, Inc.. The 510(k) number is K851070.

When did RESP-BAC BACTERIA FILTER receive FDA 510(k) clearance?

RESP-BAC BACTERIA FILTER received FDA 510(k) clearance on 1985-06-14, under 510(k) number K851070.

Who is the listed applicant for RESP-BAC BACTERIA FILTER?

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

What is the FDA product code for RESP-BAC BACTERIA FILTER?

The FDA product code for RESP-BAC BACTERIA FILTER is CAH.

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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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