The following data is part of a premarket notification filed by Philips Medical Systems with the FDA for Philips M5066a And M5068a.
| Device ID | K020715 |
| 510k Number | K020715 |
| Device Name: | PHILIPS M5066A AND M5068A |
| Classification | Automated External Defibrillators (non-wearable) |
| Applicant | PHILIPS MEDICAL SYSTEMS 2301 FIFTH AVE., SUITE 200 Seattle, WA 98121 |
| Contact | Tamara Yount |
| Correspondent | Tamara Yount PHILIPS MEDICAL SYSTEMS 2301 FIFTH AVE., SUITE 200 Seattle, WA 98121 |
| Product Code | MKJ |
| CFR Regulation Number | 870.5310 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-05 |
| Decision Date | 2002-11-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838075849 | K020715 | 000 |
| 00884838051478 | K020715 | 000 |
| 00884838050686 | K020715 | 000 |
| 00884838050679 | K020715 | 000 |
| 00884838049123 | K020715 | 000 |
| 00884838023840 | K020715 | 000 |
| 00884838023758 | K020715 | 000 |
| 00884838023741 | K020715 | 000 |