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TRAP-BLOOD VESSEL STABILIZATION DEVICE

K781072 Class II Traditional
Decision Date
1978-08-10
Sponsor / Applicant
Ayer, Patrick, M.D.

Technical Specification

510(k) Submission ID K781072
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 1978-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAP-BLOOD VESSEL STABILIZATION DEVICE received FDA 510(k) clearance under submission number K781072, sponsored by Ayer, Patrick, M.D.. 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 1978-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.