Multiple Pharma-Plast Tracheal Tube

FDA 510(k) K871263 · Pharma-Plast USA, Inc.

Substantially Equivalent

510(k) numberK871263

Submission

Device name
Multiple Pharma-Plast Tracheal Tube
Applicant
Pharma-Plast USA, Inc.
Canada H3a 2n4, CA
Received
March 31, 1987
Decision date
June 15, 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 Multiple Pharma-Plast Tracheal Tube cleared by the FDA?

Multiple Pharma-Plast Tracheal Tube (K871263) received a 510(k) decision of Substantially Equivalent on June 15, 1987, 76 days after the submission was received.

What is the product code of K871263?

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