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FDA 510(k)

RESPIR GARD BACTERIA FILTER

K-Number: K833269 · 1983-10-31

ApplicantMarquest Medical Products, Inc.
Decision Date1983-10-31
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIR GARD BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K833269. 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 RESPIR GARD BACTERIA FILTER?

RESPIR GARD BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K833269.

When did RESPIR GARD BACTERIA FILTER receive FDA 510(k) clearance?

RESPIR GARD BACTERIA FILTER received FDA 510(k) clearance on 1983-10-31, under 510(k) number K833269.

Who is the listed applicant for RESPIR GARD BACTERIA FILTER?

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

What is the FDA product code for RESPIR GARD BACTERIA FILTER?

The FDA product code for RESPIR GARD BACTERIA FILTER is CAH.

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Other records listing Marquest Medical Products, Inc. as applicant

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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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