Tube, Sterile Conductive Connecting

FDA 510(k) K760202 · Ipco Corp.

Substantially Equivalent

510(k) numberK760202

Submission

Device name
Tube, Sterile Conductive Connecting
Applicant
Ipco Corp.
Mchenry, IL, US
Received
July 8, 1976
Decision date
July 19, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GAZ – Tubing, Noninvasive
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6740
Specialty
General Hospital

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K930512Suction/Irrigation Y Tubing Set W/Trumpet ValvesGAZ · Traditional Core Dynamics, Inc.07/23/1993SE
K911865Nortec Connecting Tube SetGAZ · Traditional North American Sterilization & Packaging Co.11/01/1991SE
K910471Medid-Vac Clear Nonconductive Connecting TubeGAZ · Traditional Baxter Healthcare Corp03/08/1991SE
K910171Maxi-Flow Suction Set W/Y ConnectorGAZ · Traditional Adler Instrument Co.02/01/1991SE
K910170Maxi-Flow Suction Set 12 Ft.GAZ · Traditional Adler Instrument Co.02/01/1991SE
K882315Vir-A-Vac EmptyGAZ · Traditional Viratec Corp.09/26/1988SE
K883473Surgical Connecting TubesGAZ · Traditional Westmark, Sterile Packing Systems, Inc. (Sps)08/25/1988SE
K8649645 - in - 1 ConnectorGAZ · Traditional Medovations, Inc.01/20/1987SE

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Questions and answers

When was Tube, Sterile Conductive Connecting cleared by the FDA?

Tube, Sterile Conductive Connecting (K760202) received a 510(k) decision of Substantially Equivalent on July 19, 1976, 11 days after the submission was received.

What is the product code of K760202?

The FDA product code is GAZ – Tubing, Noninvasive, a Class II (moderate risk) device regulated under 21 CFR 880.6740.