The following data is part of a premarket notification filed by Maersk Medical A/s with the FDA for Disposable Ecg Monitoring Electrodes, Model 4110, 4140.
Device ID | K990110 |
510k Number | K990110 |
Device Name: | DISPOSABLE ECG MONITORING ELECTRODES, MODEL 4110, 4140 |
Classification | Electrode, Electrocardiograph |
Applicant | MAERSK MEDICAL A/S 6401 MEADOWS WEST Fort Worth, TX 76132 |
Contact | Richard A Hamer |
Correspondent | Richard A Hamer MAERSK MEDICAL A/S 6401 MEADOWS WEST Fort Worth, TX 76132 |
Product Code | DRX |
CFR Regulation Number | 870.2360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-01-13 |
Decision Date | 1999-12-06 |
Summary: | summary |