Suction Tubes: House, Baron

FDA 510(k) K892549 · Zinnanti Surgical Instruments, Inc.

Substantially Equivalent

510(k) numberK892549

Submission

Device name
Suction Tubes: House, Baron
Applicant
Zinnanti Surgical Instruments, Inc.
Chatsworth, CA, US
Received
April 11, 1989
Decision date
May 18, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GCX – Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6740
Specialty
General Hospital

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K972074Suction InstrumentationGCX · Traditional Walter Lorenz Surgical, Inc.07/25/1997SE
K971022Chase SuckerGCX · Traditional Chase Medical, Inc.04/17/1997SE
K964127Medi-Vac Flexi-Clear Suction HandleGCX · Traditional Allegiance Healthcare Corp.12/31/1996SE
K964519Curity Thoracentesis TrayGCX · Traditional Kendall Healthcare Products Co. Div.Of Tyco Health12/20/1996SE
K963648Stryker Suction RegulatorGCX · Traditional Stryker Endoscopy11/26/1996SE
K962920Renton Suction Device U.S. PATENT*4,767,404GCX · Traditional R&S Surgical, LLC10/21/1996SE
K961880Medcare Suction Connecting TubingGCX · Traditional Medcare Medical Group, Inc.07/19/1996SE
K960223CPR YankauerGCX · Traditional Custom Pack Reliability03/28/1996SE

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Questions and answers

When was Suction Tubes: House, Baron cleared by the FDA?

Suction Tubes: House, Baron (K892549) received a 510(k) decision of Substantially Equivalent on May 18, 1989, 37 days after the submission was received.

What is the product code of K892549?

The FDA product code is GCX – Apparatus, Suction, Operating-Room, Wall Vacuum Powered, a Class II (moderate risk) device regulated under 21 CFR 880.6740.