ECONOM

Speculum, Ent

RUDOLF RIESTER GMBH & CO. KG

The following data is part of a premarket notification filed by Rudolf Riester Gmbh & Co. Kg with the FDA for Econom.

Pre-market Notification Details

• Device ID: K925754
• 510k Number: K925754
• Device Name: ECONOM
• Classification: Speculum, Ent
• Applicant: RUDOLF RIESTER GMBH & CO. KG POSTFACH 35 BRUCKSTRABE 31 D-72417 Jungingen, DE
• Contact: Karlheinz Riester
• Correspondent: Karlheinz Riester; RUDOLF RIESTER GMBH & CO. KG POSTFACH 35 BRUCKSTRABE 31 D-72417 Jungingen, DE
• Product Code: EPY
• CFR Regulation Number: 878.1800 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-11-13
• Decision Date: 1993-10-08

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
04045396130739	K925754	000
04045396010291	K925754	000
04045396010352	K925754	000
04045396010369	K925754	000
04045396010376	K925754	000
04045396010383	K925754	000
04045396010390	K925754	000
04045396130593	K925754	000
04045396130609	K925754	000
04045396130616	K925754	000
04045396002760	K925754	000