K862848 is an FDA 510(k) clearance for the LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110. This device is classified as a Antisera, All Types, Streptococcus Pneumoniae (Class I - General Controls, product code GWC).
Submitted by Lkb Instruments, Inc. (Gaithersburg, US). The FDA issued a Cleared decision on December 18, 1986, 142 days after receiving the submission on July 29, 1986.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3740.
| 510(k) Number | K862848 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 29, 1986 |
| Decision Date | December 18, 1986 |
| Days to Decision | 142 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | GWC — Antisera, All Types, Streptococcus Pneumoniae |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.3740 |