The following data is part of a premarket notification filed by Dhd Medical Products Div. Diemolding Corp. with the FDA for Percussor.
| Device ID | K812166 |
| 510k Number | K812166 |
| Device Name: | PERCUSSOR |
| Classification | Percussor, Powered-electric |
| Applicant | DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. 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 | 1981-07-30 |
| Decision Date | 1981-08-18 |