ClearanceBrief
Company ยท US

Merrimack Laboratories

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1985. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HHRLaser, Surgical, Gynecologic2
EOQBronchoscope (Flexible Or Rigid)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 19, 1985K833528CARBON DIOXIDE LASER ML 825
Merrimack Laboratories
HHR
Feb 10, 1984K833483ENDOSCOPIC COUPLER
Merrimack Laboratories
EOQ
Sep 13, 1982K827963MODEL ML-850
Merrimack Laboratories
Jun 11, 1982K827506MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
Merrimack Laboratories
May 19, 1982K827442ML-810 CARBON DIOXIDE LASER SYSTEM
Merrimack Laboratories
Mar 3, 1980K800227ML-800 CO2
Merrimack Laboratories
HHR

Latest recalls

DateFirm and productCodeLinked 510(k)
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