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 |