OPHTHALMOSCOPE— 510(k) K925757

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K925757 for OPHTHALMOSCOPE, Substantially Equivalent on 1993-08-03. Applicant: Rudolf Riester GmbH & Co. KG.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code HLJ
Advisory panel: Ophthalmic
Date received: 1992-11-13
Decision date: 1993-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: D-72417 Jungingen, DE

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