K934271 is an FDA 510(k) clearance for the BECKMAN SYNCHRON LACTATE REAGENT. This device is classified as a Acid, Lactic, Enzymatic Method (Class I - General Controls, product code KHP).
Submitted by Beckman-Diagnostic Systems Group (Brea, US). The FDA issued a Cleared decision on November 9, 1993, 70 days after receiving the submission on August 31, 1993.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1450.
| 510(k) Number | K934271 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 31, 1993 |
| Decision Date | November 09, 1993 |
| Days to Decision | 70 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | KHP — Acid, Lactic, Enzymatic Method |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1450 |