Nasogastric Voicetube

FDA 510(k) K871632 · American Omni Medical, Inc.

Substantially Equivalent

510(k) numberK871632

Submission

Device name
Nasogastric Voicetube
Applicant
American Omni Medical, Inc.
Costa Mesa, CA, US
Received
April 27, 1987
Decision date
September 16, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTR – Tube, Tracheal (W/Wo Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5730
Specialty
Anesthesiology
Life-sustaining
Yes

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Questions and answers

When was Nasogastric Voicetube cleared by the FDA?

Nasogastric Voicetube (K871632) received a 510(k) decision of Substantially Equivalent on September 16, 1987, 142 days after the submission was received.

What is the product code of K871632?

The FDA product code is BTR – Tube, Tracheal (W/Wo Connector), a Class II (moderate risk) device regulated under 21 CFR 868.5730.