Xomed-Treace Positrol Footpedal Suction Control

FDA 510(k) K912753 · Xomed-Treace, Inc.

Substantially Equivalent

510(k) numberK912753

Submission

Device name
Xomed-Treace Positrol Footpedal Suction Control
Applicant
Xomed-Treace, Inc.
Jacksonville, FL, US
Received
June 24, 1991
Decision date
September 23, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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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K933672Xomed-Treace ScopesheathEOB · Traditional 07/18/1994SE
K934426Nerve Integrity MONITOR-2 (NIM-2 XL)ETN · Traditional 05/13/1994SE
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Questions and answers

When was Xomed-Treace Positrol Footpedal Suction Control cleared by the FDA?

Xomed-Treace Positrol Footpedal Suction Control (K912753) received a 510(k) decision of Substantially Equivalent on September 23, 1991, 91 days after the submission was received.

What is the product code of K912753?

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.