The following data is part of a premarket notification filed by Rich-mar Corp. with the FDA for Autosound 7.6 Muscle Stimulator, Tens, Therapeutic Ultrasound And Combination Device.
Device ID | K032941 |
510k Number | K032941 |
Device Name: | AUTOSOUND 7.6 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE |
Classification | Stimulator, Muscle, Powered |
Applicant | RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 -0879 |
Contact | David Richards |
Correspondent | David Richards RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 -0879 |
Product Code | IPF |
Subsequent Product Code | GZJ |
Subsequent Product Code | IMG |
Subsequent Product Code | IMI |
Subsequent Product Code | LIH |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-09-22 |
Decision Date | 2003-10-22 |