FDA 510(k)

BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING

K-Number: K881484 · 1988-05-04

Decision Date1988-05-04

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1988-05-04 under 510(k) number K881484. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING?

BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING is a medical device that received FDA 510(k) clearance on 1988-05-04. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K881484.

When did BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING receive FDA 510(k) clearance?

BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING received FDA 510(k) clearance on 1988-05-04, under 510(k) number K881484.

Who is the listed applicant for BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING?

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

What is the FDA product code for BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING?

The FDA product code for BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING is GDW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.