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SUCTION CONNECTING TUBING

K790420 Class II Traditional
Decision Date
1979-04-23
Sponsor / Applicant
Snyder Laboratories, Inc.

Technical Specification

510(k) Submission ID K790420
Product Code BYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1979-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUCTION CONNECTING TUBING received FDA 510(k) clearance under submission number K790420, sponsored by Snyder Laboratories, Inc.. 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 1979-04-23.

Classification & Regulation

This clearance is catalogued under FDA product code BYY and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.