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FDA 510(k)

DEXON 'S' POLYGLYCOLIC ACID MESH

K-Number: K830889 · 1983-05-09

ApplicantDavis & Geck, Inc.
Decision Date1983-05-09
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEXON 'S' POLYGLYCOLIC ACID MESH 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 1983-05-09 under 510(k) number K830889. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXON 'S' POLYGLYCOLIC ACID MESH?

DEXON 'S' POLYGLYCOLIC ACID MESH is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K830889.

When did DEXON 'S' POLYGLYCOLIC ACID MESH receive FDA 510(k) clearance?

DEXON 'S' POLYGLYCOLIC ACID MESH received FDA 510(k) clearance on 1983-05-09, under 510(k) number K830889.

Who is the listed applicant for DEXON 'S' POLYGLYCOLIC ACID MESH?

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 DEXON 'S' POLYGLYCOLIC ACID MESH?

The FDA product code for DEXON 'S' POLYGLYCOLIC ACID MESH is FTM.

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Other records listing Davis & Geck, 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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