Clear-Therm Micro Hme, Model 1441

FDA 510(k) K032322 · Intersurgical, Inc.

Substantially Equivalent

510(k) numberK032322

Submission

Device name
Clear-Therm Micro Hme, Model 1441
Applicant
Intersurgical, Inc.
Liverpool, NY, US
Received
July 28, 2003
Decision date
May 13, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CAH – Filter, Bacterial, Breathing-Circuit
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5260
Specialty
Anesthesiology

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More from Great Group Medical Co, Ltd.

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K121747Facefit and Facefit Ported Non-Invasive Ventilation MasksBZD · Traditional 03/14/2013SE
K122077ManometerCAP · Traditional 01/10/2013SE
K122075Disposable Gas Sampling Line with and Without In-Line FilterCCK · Traditional 12/20/2012SE
K121026Flo-Guard Breathing FilterCAH · Traditional 11/02/2012SE
K092451Intersurgical Inter-Therm Breathing Filter and Heat and Moisture Exchanger…CAH · Traditional 10/29/2010SE
K092129Intersurgical Heated Wire Breathing Systems and Humidification Chambers, Model…BZE · Traditional 05/18/2010SE
K092409Hydro-Guard Mini Breathing Filter and Heat and Moisture Exchanger and Air-Guard Clear…CAH · Traditional 03/10/2010SE

Questions and answers

When was Clear-Therm Micro Hme, Model 1441 cleared by the FDA?

Clear-Therm Micro Hme, Model 1441 (K032322) received a 510(k) decision of Substantially Equivalent on May 13, 2004, 290 days after the submission was received.

What is the product code of K032322?

The FDA product code is CAH – Filter, Bacterial, Breathing-Circuit, a Class II (moderate risk) device regulated under 21 CFR 868.5260.