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DAVID SIMMONDS ANESTHESIA EXTENSION TUBES

K905384 Class II Traditional
Decision Date
1991-03-22
Sponsor / Applicant
Sparta Surgical Corp.

Technical Specification

510(k) Submission ID K905384
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1991-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAVID SIMMONDS ANESTHESIA EXTENSION TUBES received FDA 510(k) clearance under submission number K905384, sponsored by Sparta Surgical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1991-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.