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FDA 510(k)

GASLINE FILTER, #EC-GLF SERIES

K-Number: K832935 · 1983-11-22

ApplicantGish Biomedical, Inc.
Decision Date1983-11-22
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GASLINE FILTER, #EC-GLF SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Gish Biomedical, Inc.. It received FDA 510(k) clearance on 1983-11-22 under 510(k) number K832935. 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 GASLINE FILTER, #EC-GLF SERIES?

GASLINE FILTER, #EC-GLF SERIES is a medical device that received FDA 510(k) clearance on 1983-11-22. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K832935.

When did GASLINE FILTER, #EC-GLF SERIES receive FDA 510(k) clearance?

GASLINE FILTER, #EC-GLF SERIES received FDA 510(k) clearance on 1983-11-22, under 510(k) number K832935.

Who is the listed applicant for GASLINE FILTER, #EC-GLF SERIES?

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

What is the FDA product code for GASLINE FILTER, #EC-GLF SERIES?

The FDA product code for GASLINE FILTER, #EC-GLF SERIES 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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