The following data is part of a premarket notification filed by Medical Design & Manufacturing Corp. with the FDA for Medical Designs, Inc. Bio-therapy System.
| Device ID | K911911 |
| 510k Number | K911911 |
| Device Name: | MEDICAL DESIGNS, INC. BIO-THERAPY SYSTEM |
| Classification | Device, Biofeedback |
| Applicant | MEDICAL DESIGN & MANUFACTURING CORP. 929 EASTWIND DR. Westerville, OH 43081 |
| Contact | H Southworth |
| Correspondent | H Southworth MEDICAL DESIGN & MANUFACTURING CORP. 929 EASTWIND DR. Westerville, OH 43081 |
| Product Code | HCC |
| CFR Regulation Number | 882.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-04-30 |
| Decision Date | 1992-03-20 |