The following data is part of a premarket notification filed by Rich-mar Corp. with the FDA for Rich-mar If 200.
Device ID | K854485 |
510k Number | K854485 |
Device Name: | RICH-MAR IF 200 |
Classification | Stimulator, Muscle, Powered |
Applicant | RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 |
Contact | David Richards |
Correspondent | David Richards RICH-MAR CORP. P.O. BOX 879 Inola, OK 74036 |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-11-07 |
Decision Date | 1986-06-10 |