FDA 510(k)

GASLINE FILTER #GF-10

K-Number: K832411 · 1983-09-12

Decision Date1983-09-12

Product CodeKRI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

GASLINE FILTER #GF-10 is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832411. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASLINE FILTER #GF-10?

GASLINE FILTER #GF-10 is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is American Bentley. The 510(k) number is K832411.

When did GASLINE FILTER #GF-10 receive FDA 510(k) clearance?

GASLINE FILTER #GF-10 received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832411.

Who is the listed applicant for GASLINE FILTER #GF-10?

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

What is the FDA product code for GASLINE FILTER #GF-10?

The FDA product code for GASLINE FILTER #GF-10 is KRI.

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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.