Sigma's Calcium Procedure No. 587

FDA 510(k) K871152 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK871152

Submission

Device name
Sigma's Calcium Procedure No. 587
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
March 23, 1987
Decision date
June 12, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIC – Cresolphthalein Complexone, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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Questions and answers

When was Sigma's Calcium Procedure No. 587 cleared by the FDA?

Sigma's Calcium Procedure No. 587 (K871152) received a 510(k) decision of Substantially Equivalent on June 12, 1987, 81 days after the submission was received.

What is the product code of K871152?

The FDA product code is CIC – Cresolphthalein Complexone, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.