Disposable Heated Wire Loops 48 and 72

FDA 510(k) K860941 · Intec Medical, Inc.

Substantially Equivalent

510(k) numberK860941

Submission

Device name
Disposable Heated Wire Loops 48 and 72
Applicant
Intec Medical, Inc.
Blue Springs, MO, US
Received
March 12, 1986
Decision date
April 2, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BZE – Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5270
Specialty
Anesthesiology

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Questions and answers

When was Disposable Heated Wire Loops 48 and 72 cleared by the FDA?

Disposable Heated Wire Loops 48 and 72 (K860941) received a 510(k) decision of Substantially Equivalent on April 2, 1986, 21 days after the submission was received.

What is the product code of K860941?

The FDA product code is BZE – Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer, a Class II (moderate risk) device regulated under 21 CFR 868.5270.