Company ยท US
Intl. Diagnostic, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1984. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 22, 1984 | K841853 | PREG-BETA ONE HOUR TUBE TEST Intl. Diagnostic, Inc. | JHJ |
| May 30, 1984 | K840833 | PREG BETA BLUS SLIDE Intl. Diagnostic, Inc. | JHJ |
| Feb 27, 1984 | K834584 | NABI CRP-Q.S. TEST Intl. Diagnostic, Inc. | DCN |
| Feb 13, 1984 | K840005 | NABI RF-Q.S. TEST Intl. Diagnostic, Inc. | DHR |
| Oct 10, 1980 | K802343 | PREGNA B-ANTI HUMAN CHORIONIC GONADOTRO Intl. Diagnostic, Inc. | JHJ |
| Apr 4, 1978 | K780321 | PREGNANCY TEST KIT, OVER-THE-COUNTER Intl. Diagnostic, Inc. | LCX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||