The following data is part of a premarket notification filed by B & F Medical Products, Inc. with the FDA for Hand Percussor Cup #65210.
| Device ID | K802646 |
| 510k Number | K802646 |
| Device Name: | HAND PERCUSSOR CUP #65210 |
| Classification | Percussor, Powered-electric |
| Applicant | B & F MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BYI |
| CFR Regulation Number | 868.5665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-24 |
| Decision Date | 1980-11-12 |