Aspirator, Continuous & Programmable Intermittent

FDA 510(k) K951423 · Impact Instrumentation, Inc.

Substantially Equivalent

510(k) numberK951423

Submission

Device name
Aspirator, Continuous & Programmable Intermittent
Applicant
Impact Instrumentation, Inc.
West Caldwell, NJ, US
Received
March 27, 1995
Decision date
April 18, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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K051476Uni-Vent Model 73XBTL · Traditional 10/28/2005SE
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K022062Impact, Universal Single-Limb, Ventilator Circuit, Model 820-0099-00MOD · Abbreviated 05/06/2003SE
K941096Electric Vacum PumpBTA · Traditional 01/05/1995SE
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Questions and answers

When was Aspirator, Continuous & Programmable Intermittent cleared by the FDA?

Aspirator, Continuous & Programmable Intermittent (K951423) received a 510(k) decision of Substantially Equivalent on April 18, 1995, 22 days after the submission was received.

What is the product code of K951423?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.