H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG— 510(k) K946043

Unknown

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K946043 for H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG, Unknown on 1995-03-08. 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
Decision date
Decision
Unknown
Clearance type
Traditional
Location
D-72417 Jungingen, DE
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