Company ยท US
Capintec Instruments, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1994. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Sep 29, 1994 | K943072 | BETA C COUNTER Capintec Instruments, Inc. | KPT |
| Feb 18, 1994 | K935539 | CAPINTEC CRC 35R Capintec Instruments, Inc. | KPT |
| May 18, 1993 | K930962 | CAPTUS 2000 WEL COUNTER Capintec Instruments, Inc. | IZD |
| Dec 3, 1992 | K924586 | CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWARE Capintec Instruments, Inc. | IZD |
| May 28, 1992 | K921428 | CAPTUS 500 Capintec Instruments, Inc. | IZD |
| Apr 8, 1991 | K910020 | CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS Capintec Instruments, Inc. | IZO |
| Mar 18, 1991 | K905796 | DOSE CALIBRATOR Capintec Instruments, Inc. | KPT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||