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AUTO. SAMPLING SYSTEM

K772364 Class I Traditional
Decision Date
1978-01-05
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K772364
Product Code KIE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1978-01-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO. SAMPLING SYSTEM received FDA 510(k) clearance under submission number K772364, sponsored by Hewlett-Packard Co.. 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 1978-01-05.

Classification & Regulation

This clearance is catalogued under FDA product code KIE and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.