Castle Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Castle Co. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Castle Co. has 21 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1976 to 1987.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Castle Co.
21 devices
Cleared
Apr 17, 1987
MODIFIED CASTLE POWERCLAVE
General Hospital
38d
Cleared
Mar 05, 1986
CASTLE 7538 FLOOR LOADING WASHER
General Hospital
37d
Cleared
Jan 14, 1985
CASTLE 7515 UTENSIL/GLASSWARE WASHER
General Hospital
84d
Cleared
Apr 04, 1984
BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO
General & Plastic Surgery
133d
Cleared
Nov 07, 1983
CASTLE TEC-TEST S.M.A.R.T. PACK
General Hospital
59d
Cleared
Jun 15, 1983
CASTLE MODEL 3341 & 3441 & 4141 GAS AER
General Hospital
29d
Cleared
Jan 29, 1980
UNISPORE-BIOLOGICAL INDICATORS
General Hospital
39d
Cleared
Jan 29, 1980
1500 EO EXHAUST HOOD
General Hospital
33d
Cleared
May 07, 1979
EO EVACUATING SYSTEM I
General Hospital
28d
Cleared
Dec 12, 1978
9100 DAYSTAR AND 9110 ORBITER PACKAGE
General & Plastic Surgery
35d
Cleared
Oct 27, 1978
CASTLE MODEL 3146 GAS AERATOR
General Hospital
60d
Cleared
Apr 27, 1978
DAYSTAR SELECTRA & SELECTRA/ORBITER
General & Plastic Surgery
48d