Patton, Boggs & Blow is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Patton, Boggs & Blow - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Patton, Boggs & Blow has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1994. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Patton, Boggs & Blow Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Patton, Boggs & Blow
6 devices
Cleared
Oct 04, 1994
MANUAL SURGICAL INST. AND ACC. TO KLS CHIN PLATE SYSTEM
Dental
84d
Cleared
Oct 04, 1994
MANUAL SURGICAL INST. AND ACC. TO KLS MINI OSTEOSYNTHESIS SYSTEM
Dental
84d
Cleared
Oct 04, 1994
KLS MINI OSTEOSYNTHESIS SYSTEM
Dental
84d
Cleared
Oct 04, 1994
KLS CHIN PLATE SYSTEM
Dental
84d
Cleared
Aug 16, 1983
FITKIT I CHECKUP KIT
Chemistry
424d
Cleared
Feb 24, 1983
NOSITE UV INTERIM SPECTACLES
Ophthalmic
66d