Cleared Traditional

K812670 - SANDARE FAST 340 PHOSPHORUS PROCEDURE
(FDA 510(k) Clearance)

Oct 1981
Decision
11d
Days
Class 1
Risk

K812670 is an FDA 510(k) clearance for the SANDARE FAST 340 PHOSPHORUS PROCEDURE. This device is classified as a 5-amp-phosphate Release (colorimetric Test), 5'-nucleotidase (Class I - General Controls, product code CED).

Submitted by Sandare Chemical Co., Inc. (Mchenry, US). The FDA issued a Cleared decision on October 2, 1981, 11 days after receiving the submission on September 21, 1981.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1520.

Submission Details

510(k) Number K812670 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 21, 1981
Decision Date October 02, 1981
Days to Decision 11 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CED — 5-amp-phosphate Release (colorimetric Test), 5'-nucleotidase
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1520

Similar Devices — CED 5-amp-phosphate Release (colorimetric Test), 5'-nucleotidase

All 8
PHOSPHORUS TEST ITEM NUMBER 65416
K894288 · Em Diagnostic Systems, Inc. · Aug 1989
EKTACHEM CLINICAL CHEM. SLIDES
K840151 · Eastman Kodak Company · Mar 1984
BTC URINE LH ASSAY
K833710 · Btc Diagnostics, Inc. · Jan 1984
PHOSPHORUS IL
K820832 · American Monitor Corp. · Apr 1982
SIGMA PROCEDURE 265-UV
K811864 · Sigma Chemical Co. · Jul 1981
INORGANIC PHOSPHORUS REAGENTS
K811222 · Connecticut Diagnostics, Ltd. · May 1981