Cleared Traditional

FINNIGAN MAT INCOS 50

K873603 · Finnigan Corp. · Chemistry
Sep 1987
Decision
18d
Days
Class 1
Risk

About This 510(k) Submission

K873603 is an FDA 510(k) clearance for the FINNIGAN MAT INCOS 50, a Flame Emission Photometer For Clinical Use (Class I — General Controls, product code JJO), submitted by Finnigan Corp. (San Jose, US). The FDA issued a Cleared decision on September 22, 1987, 18 days after receiving the submission on September 4, 1987. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2540.

Submission Details

510(k) Number K873603 FDA.gov
FDA Decision Cleared SESE
Date Received September 04, 1987
Decision Date September 22, 1987
Days to Decision 18 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

Product Code JJO — Flame Emission Photometer For Clinical Use
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.2540