The following data is part of a premarket notification filed by Zoll Medical Corp. with the FDA for Zoll M Series Etco2 Option.
| Device ID | K993036 |
| 510k Number | K993036 |
| Device Name: | ZOLL M SERIES ETCO2 OPTION |
| 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 |
| CFR Regulation Number | 870.5310 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-09-09 |
| Decision Date | 2000-02-28 |