Santa Barbara Medco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Santa Barbara Medco, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Santa Barbara Medco, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1980 to 1985. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Santa Barbara Medco, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Santa Barbara Medco, Inc.
8 devices
Cleared
Mar 07, 1985
NASAL SEPTAL BUTTON
Ear, Nose, Throat
27d
Cleared
Aug 31, 1984
SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC
Physical Medicine
67d
Cleared
Mar 28, 1983
PHYSICIANS CHOICE SILICONE EAR PUTTY
Ear, Nose, Throat
90d
Cleared
May 27, 1982
MEDCO CUSTOM EAR PROTECTOR MOLD KIT
Ear, Nose, Throat
30d
Cleared
Aug 31, 1981
BORES* DEPTH GAUGE
General & Plastic Surgery
41d
Cleared
Aug 31, 1981
RK IV SURGICAL BLADES
General & Plastic Surgery
41d
Cleared
Aug 18, 1981
BORES* ADJUSTABLE BLADE HOLDER
General & Plastic Surgery
28d
Cleared
Nov 12, 1980
OTOLOGICAL VENTILATION TUBES
Ear, Nose, Throat
21d