The following data is part of a premarket notification filed by Bio-detek, Inc. with the FDA for Zoll Superpadz Adult Multi-function Electrodes, Model 8900-xxxx.
Device ID | K984582 |
510k Number | K984582 |
Device Name: | ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX |
Classification | Automated External Defibrillators (non-wearable) |
Applicant | BIO-DETEK, INC. 525 NARRAGANSETT PARK DR. Pawtucket, RI 02861 -4323 |
Contact | Michael R Dupelle |
Correspondent | Michael R Dupelle BIO-DETEK, INC. 525 NARRAGANSETT PARK DR. Pawtucket, RI 02861 -4323 |
Product Code | MKJ |
CFR Regulation Number | 870.5310 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-12-23 |
Decision Date | 1999-03-16 |