Company ยท US
Intracel Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2000. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Nov 7, 2000 | K003204 | BARTELS VIRAL RESPIRATORY SCREENING AND IDENTIFICATION KIT Intracel Corp. | GNW |
| Dec 21, 1999 | K991074 | BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST Intracel Corp. | MJH |
| Mar 31, 1999 | K990664 | PRIMA SYSTEM - OLD, BARTELS ELISA - NEW Intracel Corp. | LLH |
| Dec 14, 1998 | K982311 | BARTELS CINAKIT CMV ANTIGENEMIA Intracel Corp. | GQH |
| Nov 14, 1995 | K933878 | ZYMMUNE(TM) CD4/CD8 CELL MONITORING KIT Intracel Corp. | GKZ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||