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FDA 510(k)

SURGILON, DERMALON, & OPHTHALON

K-Number: K981582 · 1998-07-13

ApplicantDavis & Geck, Inc.
Decision Date1998-07-13
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGILON, DERMALON, & OPHTHALON 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 1998-07-13 under 510(k) number K981582. The device is classified under product code GAR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGILON, DERMALON, & OPHTHALON?

SURGILON, DERMALON, & OPHTHALON is a medical device that received FDA 510(k) clearance on 1998-07-13. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K981582.

When did SURGILON, DERMALON, & OPHTHALON receive FDA 510(k) clearance?

SURGILON, DERMALON, & OPHTHALON received FDA 510(k) clearance on 1998-07-13, under 510(k) number K981582.

Who is the listed applicant for SURGILON, DERMALON, & OPHTHALON?

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 SURGILON, DERMALON, & OPHTHALON?

The FDA product code for SURGILON, DERMALON, & OPHTHALON is GAR.

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Related Devices (Code: GAR)

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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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