The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Quik-pace(r) Or Ex-pace(tm) Pediatric Pacing Elec.
Device ID | K912599 |
510k Number | K912599 |
Device Name: | QUIK-PACE(R) OR EX-PACE(TM) PEDIATRIC PACING ELEC |
Classification | Pacemaker, Cardiac, External Transcutaneous (non-invasive) |
Applicant | PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Contact | Sherri L Pocock |
Correspondent | Sherri L Pocock PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Product Code | DRO |
CFR Regulation Number | 870.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-10 |
Decision Date | 1991-09-11 |