Edward Weck, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WECK TROCAR, LM15(TM), CATALOG NUMBER - 523821, HEMOCLIP II
140
Total
140
Cleared
0
Denied
FDA 510(k) Regulatory Record - Edward Weck, Inc. Ear, Nose, Throat ✕
17 devices
Cleared
Feb 10, 1984
PULSATRON NERVE LOCATOR/STIMULATOR
Ear, Nose, Throat
116d
Cleared
Aug 12, 1980
FRAZIER-FERGUSON SUCTION TUBES
Ear, Nose, Throat
49d
Cleared
Feb 21, 1980
NASOSTAT
Ear, Nose, Throat
24d
Cleared
Feb 27, 1978
DAY HEAR HOOK
Ear, Nose, Throat
6d
Cleared
Feb 02, 1978
JOSEPH SAW
Ear, Nose, Throat
37d
Cleared
Jan 17, 1978
ROLLER KNIFE
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
HILDYARD POST NASAL FORCEP
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
RING HANDLE & RETRACTORS
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
MYRINGOTOMY KNIFE
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
DAY EAR HOOK
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
BOIES NASAL FRACTURE ELEVATOR
Ear, Nose, Throat
21d
Cleared
Jan 17, 1978
ALLPORT MASTOID RETRACTORS
Ear, Nose, Throat
21d