K855234 is an FDA 510(k) clearance for the DIAGNOSTIC REAGENT VET-RPLA. This device is classified as a Antisera, All Types, Escherichia Coli (Class I - General Controls, product code GNA).
Submitted by Oxoid U.S.A., Inc. (Columbia, US). The FDA issued a Cleared decision on November 4, 1986, 308 days after receiving the submission on December 31, 1985.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3255.
| 510(k) Number | K855234 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 31, 1985 |
| Decision Date | November 04, 1986 |
| Days to Decision | 308 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | GNA — Antisera, All Types, Escherichia Coli |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.3255 |