The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Low Energy Dc - Defibrillator (including Paddles).
Device ID | K895379 |
510k Number | K895379 |
Device Name: | LOW ENERGY DC - DEFIBRILLATOR (INCLUDING PADDLES) |
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 | 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 | LDD |
CFR Regulation Number | 870.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-30 |
Decision Date | 1990-02-26 |