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. Device class: 2.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
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 ↗

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More clearances from Rudolf Riester GmbH & Co. KG

K002954 — RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERS2000-12-21
K002955 — EMPIRE N BLOOD PRESSURE MANOMETERS2000-12-21
K972377 — RI-MEGA1997-09-24
K972378 — SANAPHON N1997-09-24
K972379 — PRECISA N1997-09-24

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