Mdt Corp., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mdt Corp., Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Mdt Corp., Inc. has 22 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1979 to 1996.
Browse the FDA 510(k) cleared devices submitted by Mdt Corp., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mdt Corp., Inc.
22 devices
Cleared
May 23, 1996
MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR
General Hospital
87d
Cleared
Aug 26, 1994
MDT UROLOGY TABLE
Gastroenterology & Urology
93d
Cleared
Aug 10, 1994
IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLE
General & Plastic Surgery
77d
Cleared
Feb 16, 1994
MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
General Hospital
534d
Cleared
Jan 26, 1994
DENTAL LIGHT
Dental
421d
Cleared
Oct 15, 1993
MDT/HARVEY MC-8 AND MC-10
General Hospital
380d
Cleared
Jul 21, 1993
BOVIE ULTRASONIC SURGICAL ASPIRATOR
General & Plastic Surgery
82d
Cleared
May 20, 1993
MDT DENTAL CHAIR
Dental
73d
Cleared
Mar 31, 1993
MDT/CASTLE 10/90 DUAL LOAD STATION
General Hospital
397d
Cleared
Aug 10, 1992
MDT CASTLE BIOSIGN TEST PACK
General Hospital
90d
Cleared
Dec 19, 1991
MDT/SHAMPAINE MODEL 4900B SURGICAL TABLE
General & Plastic Surgery
58d
Cleared
Dec 17, 1991
MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE
General & Plastic Surgery
18d