The following data is part of a premarket notification filed by Zimmer Elektromedizin Gmbh with the FDA for Vaco Suction Electrode Unit.
Device ID | K860758 |
510k Number | K860758 |
Device Name: | VACO SUCTION ELECTRODE UNIT |
Classification | Stimulator, Muscle, Powered |
Applicant | ZIMMER ELEKTROMEDIZIN GMBH JUNKERSSTRABE 9 POSTFACH 22 80 7910 Neu-ulm, Germany, DE |
Contact | Wolfgang Kunze |
Correspondent | Wolfgang Kunze ZIMMER ELEKTROMEDIZIN GMBH JUNKERSSTRABE 9 POSTFACH 22 80 7910 Neu-ulm, Germany, DE |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-28 |
Decision Date | 1986-05-02 |