Palmetto Chemical & Supply Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palmetto Chemical & Supply Co., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Palmetto Chemical & Supply Co., Inc. has 6 FDA 510(k) cleared medical devices. Based in Monroe, US.
Historical record: 6 cleared submissions from 1986 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Palmetto Chemical & Supply Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Palmetto Chemical & Supply Co., Inc.
6 devices
Cleared
Jun 17, 1986
WECK INSTRUMENT CLEANER, CAT. NO. 850-103
General Hospital
49d
Cleared
Jun 17, 1986
WEC-KLEEN, CATALOG N. 850-102
General Hospital
49d
Cleared
Jun 17, 1986
WEC-WASH, CATALOG NO. 850-115
General Hospital
49d
Cleared
May 23, 1986
WECK-KREEM, CATALOG NO. 850-155
General & Plastic Surgery
24d
Cleared
May 23, 1986
WECK-LUBE, CATALOG NO. 850-150
General & Plastic Surgery
24d
Cleared
May 19, 1986
WECK CONCENTRATED LIQUID CLEANER
General Hospital
20d