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FDA 510(k)

SURGICAL/LID MARGIN COVER & EYELASH-

K-Number: K831285 · 1983-06-03

ApplicantRichard R. Anthony, M.D.
Decision Date1983-06-03
Product CodeHOD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SURGICAL/LID MARGIN COVER & EYELASH- is the device name listed in this FDA 510(k) record. The listed applicant is Richard R. Anthony, M.D.. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K831285. The device is classified under product code HOD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL/LID MARGIN COVER & EYELASH-?

SURGICAL/LID MARGIN COVER & EYELASH- is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Richard R. Anthony, M.D.. The 510(k) number is K831285.

When did SURGICAL/LID MARGIN COVER & EYELASH- receive FDA 510(k) clearance?

SURGICAL/LID MARGIN COVER & EYELASH- received FDA 510(k) clearance on 1983-06-03, under 510(k) number K831285.

Who is the listed applicant for SURGICAL/LID MARGIN COVER & EYELASH-?

The FDA 510(k) record lists Richard R. Anthony, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL/LID MARGIN COVER & EYELASH-?

The FDA product code for SURGICAL/LID MARGIN COVER & EYELASH- is HOD.

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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.

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