Medical Device Manufacturer · US , Sylmar , CA

Maersk Medical A/S - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1998

Total

Cleared

Denied

Maersk Medical A/S has 9 FDA 510(k) cleared medical devices. Based in Sylmar, US.

Historical record: 9 cleared submissions from 1998 to 2001. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Maersk Medical A/S Filter by specialty or product code using the sidebar.

Maersk Medical A/S is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Maersk Medical A/S

9 devices

1-9 of 9

Cleared Jun 07, 2001

PARADIGM QUICK-SET INFUSION SET

K011071 · FPA

General Hospital · 59d

Cleared Aug 29, 2000

PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380

K002138 · FPA

General Hospital · 43d

Cleared Dec 06, 1999

DISPOSABLE ECG MONITORING ELECTRODES, MODEL 4110, 4140

K990110 · DRX

Cardiovascular · 327d

Cleared Dec 06, 1999

DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4520, 4535, 4570

K990111 · DRX

Cardiovascular · 327d

Cleared Dec 06, 1999

DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4060, 4610

K990112 · DRX

Cardiovascular · 327d

Cleared Dec 06, 1999

DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4500,4530, 4533, 4539, 4540, AND...

K990113 · DRX

Cardiovascular · 327d

Cleared Dec 06, 1999

DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440

K990115 · DRX

Cardiovascular · 327d

Cleared Jun 25, 1999

MAERSK MEDICAL CONTOUR INFUSION SET

K991759 · FPA

General Hospital · 32d

Cleared Mar 17, 1998

4L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAG

K973364 · KNX

Gastroenterology & Urology · 190d

Maersk Medical A/S - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Maersk Medical A/S

Filters