Philadelphia Medical Specialties is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philadelphia Medical Specialties - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Philadelphia Medical Specialties has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1984. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Philadelphia Medical Specialties Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philadelphia Medical Specialties
6 devices
Cleared
Apr 04, 1984
PHILLY INFANT BOLT
Neurology
26d
Cleared
Feb 10, 1984
PHILLY BOLTS
Neurology
86d
Cleared
Dec 22, 1982
PHILLY BOLT ADULT PROCEDURE KIT
Neurology
34d
Cleared
Sep 14, 1982
CLASS II DEVICE FOR I.C.P. MONITORING
Neurology
14d
Cleared
Jan 28, 1982
PHILLY INFANT BOLT
Neurology
9d
Cleared
Dec 18, 1981
PHILLY BOLT
Neurology
10d