The following data is part of a premarket notification filed by Deschutes Medical Products, Inc. with the FDA for Reflex Treatment System.
| Device ID | K994079 |
| 510k Number | K994079 |
| Device Name: | REFLEX TREATMENT SYSTEM |
| Classification | Perineometer |
| Applicant | DESCHUTES MEDICAL PRODUCTS, INC. 1011 S.W. EMKAY DR., SUITE 104 Bend, OR 97702 |
| Contact | Denise Bestwick |
| Correspondent | Denise Bestwick DESCHUTES MEDICAL PRODUCTS, INC. 1011 S.W. EMKAY DR., SUITE 104 Bend, OR 97702 |
| Product Code | HIR |
| CFR Regulation Number | 884.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-12-02 |
| Decision Date | 2000-03-01 |
| Summary: | summary |