The following data is part of a premarket notification filed by Zoll Medical Corp. with the FDA for Zoll M Series With Rectilinear Bi-phasic Option (m Series Bi-phasic).
Device ID | K990762 |
510k Number | K990762 |
Device Name: | ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC) |
Classification | Automated External Defibrillators (non-wearable) |
Applicant | ZOLL MEDICAL CORP. 32 SECOND AVE. Burlington, MA 01803 |
Contact | Paul Dias |
Correspondent | Paul Dias ZOLL MEDICAL CORP. 32 SECOND AVE. Burlington, MA 01803 |
Product Code | MKJ |
Subsequent Product Code | DPS |
Subsequent Product Code | DRO |
Subsequent Product Code | LDD |
CFR Regulation Number | 870.5310 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-03-08 |
Decision Date | 1999-09-03 |