FDA 510(k)

BONGORT ODOR BARRIER DRAIN

K-Number: K792381 · 1979-12-10

Decision Date1979-12-10

Product CodeEXB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BONGORT ODOR BARRIER DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792381. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONGORT ODOR BARRIER DRAIN?

BONGORT ODOR BARRIER DRAIN is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Howmedica Corp.. The 510(k) number is K792381.

When did BONGORT ODOR BARRIER DRAIN receive FDA 510(k) clearance?

BONGORT ODOR BARRIER DRAIN received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792381.

Who is the listed applicant for BONGORT ODOR BARRIER DRAIN?

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

What is the FDA product code for BONGORT ODOR BARRIER DRAIN?

The FDA product code for BONGORT ODOR BARRIER DRAIN is EXB.

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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.