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PROCESSOR, K750 COMPUTER/DATA

K782052 Class I Traditional
Decision Date
1979-01-17
Sponsor / Applicant
Kallestad Laboratories, Inc.

Technical Specification

510(k) Submission ID K782052
Product Code JQP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2100
Decision Date 1979-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCESSOR, K750 COMPUTER/DATA received FDA 510(k) clearance under submission number K782052, sponsored by Kallestad Laboratories, 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 1979-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code JQP and 21 CFR 862.2100, within the Clinical Chemistry review panel as a Class I device.