The following data is part of a premarket notification filed by Med Systems with the FDA for Electro Flo Percussor, Model 5000.
| Device ID | K031876 |
| 510k Number | K031876 |
| Device Name: | ELECTRO FLO PERCUSSOR, MODEL 5000 |
| Classification | Percussor, Powered-electric |
| Applicant | MED SYSTEMS PO BOX 7007 Deerfield, IL 60015 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm MED SYSTEMS PO BOX 7007 Deerfield, IL 60015 |
| Product Code | BYI |
| CFR Regulation Number | 868.5665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-06-17 |
| Decision Date | 2003-11-21 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00862528000302 | K031876 | 000 |