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STOPCOCKS, MANIFOLDS

K782095 Class II Traditional
Decision Date
1979-01-23
Sponsor / Applicant
Namic

Technical Specification

510(k) Submission ID K782095
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 1979-01-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STOPCOCKS, MANIFOLDS received FDA 510(k) clearance under submission number K782095, sponsored by Namic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1979-01-23.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.