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LANCER AUTOANALYZER MANIFOLD PUMP TUB

K760622 Class I Traditional
Decision Date
1976-11-24
Sponsor / Applicant
Sherwood Medical Industries

Technical Specification

510(k) Submission ID K760622
Product Code JJC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2150
Decision Date 1976-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LANCER AUTOANALYZER MANIFOLD PUMP TUB received FDA 510(k) clearance under submission number K760622, sponsored by Sherwood Medical Industries. 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 1976-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code JJC and 21 CFR 862.2150, within the Clinical Chemistry review panel as a Class I device.