The following data is part of a premarket notification filed by Smith And Nephew Donjoy, Inc. with the FDA for Musclemax Plus Electrical Muscle Stimulator.
Device ID | K962462 |
510k Number | K962462 |
Device Name: | MUSCLEMAX PLUS ELECTRICAL MUSCLE STIMULATOR |
Classification | Stimulator, Muscle, Powered |
Applicant | SMITH AND NEPHEW DONJOY, INC. 2777 LOKER AVENUE WEST Carsbad, CA 92008 -6601 |
Contact | Dan W Miller |
Correspondent | Dan W Miller SMITH AND NEPHEW DONJOY, INC. 2777 LOKER AVENUE WEST Carsbad, CA 92008 -6601 |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-06-25 |
Decision Date | 1996-09-23 |
Summary: | summary |