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SANDARE NITROPRUSSIDE TEST PROCEDURE

K810514 Class I Traditional
Decision Date
1981-03-04
Sponsor / Applicant
Sandare Chemical Co., Inc.

Technical Specification

510(k) Submission ID K810514
Product Code JLC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1240
Decision Date 1981-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SANDARE NITROPRUSSIDE TEST PROCEDURE received FDA 510(k) clearance under submission number K810514, sponsored by Sandare Chemical Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1981-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code JLC and 21 CFR 862.1240, within the Clinical Chemistry review panel as a Class I device.