The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Fast-patch(tm).
Device ID | K871224 |
510k Number | K871224 |
Device Name: | FAST-PATCH(TM) |
Classification | Dc-defibrillator, Low-energy, (including Paddles) |
Applicant | PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Contact | Gail E Nova |
Correspondent | Gail E Nova PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Product Code | LDD |
CFR Regulation Number | 870.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-27 |
Decision Date | 1987-05-20 |