K861303 is an FDA 510(k) clearance for the GLUCOMETER II IMPROVED REFLECTANCE PHOTOMETER. This device is classified as a Glucose Oxidase, Glucose (Class II - Special Controls, product code CGA).
Submitted by Miles Laboratories, Inc. (Elkhart, US). The FDA issued a Cleared decision on July 2, 1986, 86 days after receiving the submission on April 7, 1986.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1345.
| 510(k) Number | K861303 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 07, 1986 |
| Decision Date | July 02, 1986 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CGA — Glucose Oxidase, Glucose |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1345 |