• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K781892, LOCATOR, FOREIGN BODY, by Keeler Optical Products , Ltd.

FDA 510(k) K781892, LOCATOR, FOREIGN BODY, by Keeler Optical Products , Ltd.

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510(K) Number: K781892
Device Name: LOCATOR, FOREIGN BODY
Manufacturer: Keeler Optical Products , Ltd.
Device Classification Name: locator, metal, electronic
Regulation Number: 886.4400
Classification Product Code: HPM
Date Received: 11/08/1978
Decision Date: 12/04/1978
Regulation Medical Specialty: Ophthalmic
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