The following data is part of a premarket notification filed by Merced Medical, Inc. with the FDA for Mj Percussor(tm).
| Device ID | K901026 |
| 510k Number | K901026 |
| Device Name: | MJ PERCUSSOR(TM) |
| Classification | Percussor, Powered-electric |
| Applicant | MERCED MEDICAL, INC. 113300 A-49TH ST. NORTH Clearwater, FL 34622 |
| Contact | Jeff Ratner |
| Correspondent | Jeff Ratner MERCED MEDICAL, INC. 113300 A-49TH ST. NORTH Clearwater, FL 34622 |
| Product Code | BYI |
| CFR Regulation Number | 868.5665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-03-06 |
| Decision Date | 1990-03-15 |