RI-FORMER— 510(k) K932504

Unknown

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K932504 for RI-FORMER, Unknown on 1993-10-15. Applicant: Rudolf Riester GmbH & Co. KG.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code HLJ
Advisory panel: Ophthalmic
Date received: 1993-05-21
Decision date: 1993-10-15
Decision: Unknown
Clearance type: Traditional
Location: D-72417 Jungingen, DE

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.