Cleared Traditional

K970984 - THE ELECSYS CALCHECK PROGESTERONE (FDA 510(k) Clearance)

Apr 1997
Decision
16d
Days
Class 1
Risk

K970984 is an FDA 510(k) clearance for the THE ELECSYS CALCHECK PROGESTERONE. This device is classified as a Single (specified) Analyte Controls (assayed And Unassayed) (Class I - General Controls, product code JJX).

Submitted by Boehringer Mannheim Corp. (Concord, US). The FDA issued a Cleared decision on April 2, 1997, 16 days after receiving the submission on March 17, 1997.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1660.

Submission Details

510(k) Number K970984 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 1997
Decision Date April 02, 1997
Days to Decision 16 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code JJX — Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1660