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FDA 510(k)

PERIOGRAF DURAPATITE 40-60 MESH

K-Number: K840260 · 1984-04-05

ApplicantSterling Drug, Inc.
Decision Date1984-04-05
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIOGRAF DURAPATITE 40-60 MESH is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Drug, Inc.. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K840260. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIOGRAF DURAPATITE 40-60 MESH?

PERIOGRAF DURAPATITE 40-60 MESH is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Sterling Drug, Inc.. The 510(k) number is K840260.

When did PERIOGRAF DURAPATITE 40-60 MESH receive FDA 510(k) clearance?

PERIOGRAF DURAPATITE 40-60 MESH received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840260.

Who is the listed applicant for PERIOGRAF DURAPATITE 40-60 MESH?

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

What is the FDA product code for PERIOGRAF DURAPATITE 40-60 MESH?

The FDA product code for PERIOGRAF DURAPATITE 40-60 MESH is LYC.

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Other records listing Sterling Drug, Inc. as applicant

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Related Devices (Code: LYC)

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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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