Merrimack Laboratories - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Merrimack Laboratories has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1980 to 1985. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Merrimack Laboratories Filter by specialty or product code using the sidebar.
6 devices
Cleared
Feb 19, 1985
CARBON DIOXIDE LASER ML 825
Obstetrics & Gynecology
515d
Cleared
Feb 10, 1984
ENDOSCOPIC COUPLER
Ear, Nose, Throat
126d
Cleared
Sep 13, 1982
MODEL ML-850
Radiology
24d
Cleared
Jun 11, 1982
MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
Radiology
38d
Cleared
May 19, 1982
ML-810 CARBON DIOXIDE LASER SYSTEM
Radiology
33d
Cleared
Mar 03, 1980
ML-800 CO2
Obstetrics & Gynecology
27d