SUCTION CONNECTING TUBING— 510(k) K790420

Name: FDA 510(k) clearance K790420
Creator: U.S. Food and Drug Administration
Published: 1979-04-23

Substantially Equivalent

Snyder Laboratories, Inc.

FDA 510(k) clearance K790420 for SUCTION CONNECTING TUBING, Substantially Equivalent on 1979-04-23. Applicant: Snyder Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Snyder Laboratories, Inc.
Product code: Code BYY
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1979-02-28
Decision date: 1979-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYY

view all

K960616 — VITAFLOW SUCTION/ASPIRATION TUBING SET1996-05-06
K960218 — CONNECTING TUBING1996-03-28
K955149 — MAXI-FLOW SUCTION HANDLE/THE REEL THING TUBING REEL1996-01-24
K955151 — MAXI-FLOW SUCTION TUBE/TOP GUN SUCTION IRRIGATOR1996-01-24
K955150 — MAXI-FLOW1996-01-23

More clearances from Snyder Laboratories, Inc.

view all

K843906 — SNYDER HEMOVAC WOUND DRAINAGE DEVICES1984-11-05
K821321 — SNYDER DEBRIBEMENT SYSTEM LDP-11982-08-06
K800861 — SNYDER HEMOVAC CHEST DRAINAGE SOLUTION1980-05-02
K800543 — SNYDER HYSTERECTOMY Y TUBE KIT1980-04-16
K800577 — SNYDER HEMOVAC TM VENTED WOUND KIT1980-04-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.