Cleared Traditional

K810356 - BICARBONATE TEST (FDA 510(k) Clearance)

Feb 1981
Decision
13d
Days
Class 2
Risk

K810356 is an FDA 510(k) clearance for the BICARBONATE TEST. This device is classified as a Enzymatic, Carbon-dioxide (Class II - Special Controls, product code KHS).

Submitted by Boehringer Mannheim Corp. (Mchenry, US). The FDA issued a Cleared decision on February 23, 1981, 13 days after receiving the submission on February 10, 1981.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1160.

Submission Details

510(k) Number K810356 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 10, 1981
Decision Date February 23, 1981
Days to Decision 13 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code KHS — Enzymatic, Carbon-dioxide
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1160