Cleared Traditional

K810464 - EMIT-ST SERUM CALBRATOR (FDA 510(k) Clearance)

Mar 1981
Decision
11d
Days
Class 2
Risk

K810464 is an FDA 510(k) clearance for the EMIT-ST SERUM CALBRATOR. This device is classified as a Calibrators, Drug Mixture (Class II - Special Controls, product code DKB).

Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on March 6, 1981, 11 days after receiving the submission on February 23, 1981.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3200.

Submission Details

510(k) Number K810464 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 23, 1981
Decision Date March 06, 1981
Days to Decision 11 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary

Device Classification

Product Code DKB — Calibrators, Drug Mixture
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3200