The following data is part of a premarket notification filed by Moeller Medical Gmbh & Co. Kg with the FDA for Liposat Basic (infiltration Pump), Model 92-007 688.
Device ID | K072793 |
510k Number | K072793 |
Device Name: | LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 |
Classification | System, Suction, Lipoplasty |
Applicant | MOELLER MEDICAL GMBH & CO. KG 23832 VIA MONTE Coto De Caza, CA 92679 -4001 |
Contact | Bill Kelley |
Correspondent | Bill Kelley MOELLER MEDICAL GMBH & CO. KG 23832 VIA MONTE Coto De Caza, CA 92679 -4001 |
Product Code | MUU |
CFR Regulation Number | 878.5040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-01 |
Decision Date | 2008-03-04 |
Summary: | summary |