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ABSOLUTE(TM)-HCG URINE PREGNANCY TEST

K893953 Class II Traditional
Decision Date
1989-08-15
Sponsor / Applicant
Totem Diagnostics, Inc.

Technical Specification

510(k) Submission ID K893953
Product Code DHA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1989-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABSOLUTE(TM)-HCG URINE PREGNANCY TEST received FDA 510(k) clearance under submission number K893953, sponsored by Totem Diagnostics, 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 1989-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code DHA and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.