RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT— 510(k) K964338

Name: FDA 510(k) clearance K964338
Creator: U.S. Food and Drug Administration
Published: 1997-01-09

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K964338 for RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT, Substantially Equivalent on 1997-01-09. Applicant: Rudolf Riester GmbH & Co. KG. Device class: 1.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code HKM
Device class: Class 1
Regulation: 21 CFR 886.1780
Advisory panel: Ophthalmic
Date received: 1996-10-31
Decision date: 1997-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: D-72417 Jungingen, DE

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K950795 — STREAK RETINOSCOPE RX-RP1995-03-28

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