RI-SCOPE (S)— 510(k) K932506

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K932506 for RI-SCOPE (S), Substantially Equivalent on 1993-10-08. Applicant: Rudolf Riester GmbH & Co. KG. Device class: 1.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code ERA
Device class: Class 1
Regulation: 21 CFR 874.4770
Advisory panel: Ear, Nose, Throat
Date received: 1993-05-21
Decision date: 1993-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: D-72417 Jungingen, DE

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Recent devices under product code ERA

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K121326 — LANTOS 3D EAR SCANNER2013-01-25
K110326 — OSRAM ITOS2011-10-27
K945264 — OPTUS OTOSCOPES1996-02-02
K955043 — WELCH ALLYN BI-OTOSCOPE1995-11-14

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.