Inter-Therm Pediatric Hmef, Intern-Therm Mini Pediatric Angled Hmef

FDA 510(k) K141087 · Intersurgical Incorporated

Substantially Equivalent

510(k) numberK141087

Submission

Device name
Inter-Therm Pediatric Hmef, Intern-Therm Mini Pediatric Angled Hmef
Applicant
Intersurgical Incorporated
Liverpool, NY, US
Received
April 28, 2014
Decision date
February 12, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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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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
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Questions and answers

When was Inter-Therm Pediatric Hmef, Intern-Therm Mini Pediatric Angled Hmef cleared by the FDA?

Inter-Therm Pediatric Hmef, Intern-Therm Mini Pediatric Angled Hmef (K141087) received a 510(k) decision of Substantially Equivalent on February 12, 2015, 290 days after the submission was received.

What is the product code of K141087?

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