Oscilflator

FDA 510(k) K952566 · Surgical Technologies, Inc.

Substantially Equivalent

510(k) numberK952566

Submission

Device name
Oscilflator
Applicant
Surgical Technologies, Inc.
Salt Lake City, UT, US
Received
June 2, 1995
Decision date
August 31, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MAV – Syringe, Balloon Inflation
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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K152387Fluent Inflation DeviceMAV · Traditional Vascular Solutions, Inc.12/18/2015SESK
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K140745Encore 26 Advantage KitMAV · Special Boston Scientific Corp04/17/2014SESK

More from Boston Scientific Corp

510(k)DeviceDecision
K941992CystoscopeFBO · Traditional 11/30/1995SE
K942029ArthroscopeHRX · Traditional 11/08/1995SE
K946136Infinitech Lighted Infusion CannulaMPA · Traditional 10/02/1995SE
K951918Surgical Technologies, Inc. SyringeFMF · Traditional 07/20/1995SE
K950683Arthrogram TrayJAA · Traditional 05/06/1995SE
K946135Infinitech Aspirating Laser ProbeHQE · Traditional 04/18/1995SE
K946181Infinitech Soft Tip Flute NeedleHQE · Traditional 03/14/1995SE
K942030Biopsy ScissorsOCZ · Traditional 06/27/1994SE
K942482Pressure Monitoring ExtensionDQO · Traditional 06/14/1994SE
K941161Flexible Grasping ForcepsEOQ · Traditional 05/04/1994SE

Questions and answers

When was Oscilflator cleared by the FDA?

Oscilflator (K952566) received a 510(k) decision of Substantially Equivalent on August 31, 1995, 90 days after the submission was received.

What is the product code of K952566?

The FDA product code is MAV – Syringe, Balloon Inflation, a Class II (moderate risk) device regulated under 21 CFR 870.1650.