The following data is part of a premarket notification filed by Padpro Llc. with the FDA for Padpro, Model 2502.
| Device ID | K020743 |
| 510k Number | K020743 |
| Device Name: | PADPRO, MODEL 2502 |
| Classification | Automated External Defibrillators (non-wearable) |
| Applicant | PADPRO LLC. P.O.BOX 7007 Deerfield, IL 60015 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm PADPRO LLC. P.O.BOX 7007 Deerfield, IL 60015 |
| Product Code | MKJ |
| CFR Regulation Number | 870.5310 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-06 |
| Decision Date | 2002-05-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20653405042713 | K020743 | 000 |
| 20653405042614 | K020743 | 000 |
| 20653405042515 | K020743 | 000 |
| 20653405040054 | K020743 | 000 |