Intl. Diagnostic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Diagnostic, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Intl. Diagnostic, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1984. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Intl. Diagnostic, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Diagnostic, Inc.
6 devices
Cleared
Jun 22, 1984
PREG-BETA ONE HOUR TUBE TEST
Chemistry
50d
Cleared
May 30, 1984
PREG BETA BLUS SLIDE
Chemistry
96d
Cleared
Feb 27, 1984
NABI CRP-Q.S. TEST
Immunology
60d
Cleared
Feb 13, 1984
NABI RF-Q.S. TEST
Immunology
40d
Cleared
Oct 10, 1980
PREGNA B-ANTI HUMAN CHORIONIC GONADOTRO
Chemistry
14d
Cleared
Apr 04, 1978
PREGNANCY TEST KIT, OVER-THE-COUNTER
Chemistry
39d