Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, Sterile

FDA 510(k) K955564 · Rusch, Inc.

Substantially Equivalent

510(k) numberK955564

Submission

Device name
Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, Sterile
Applicant
Rusch, Inc.
Jeffrey, NH, US
Received
December 6, 1995
Decision date
June 28, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOH – Tube Tracheostomy And Tube Cuff
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5800
Specialty
Anesthesiology
Life-sustaining
Yes

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K963993Rusch Simplastic Foley Catheterization SetFCM · Traditional 12/17/1996SE
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Questions and answers

When was Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, Sterile cleared by the FDA?

Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, Sterile (K955564) received a 510(k) decision of Substantially Equivalent on June 28, 1996, 205 days after the submission was received.

What is the product code of K955564?

The FDA product code is JOH – Tube Tracheostomy And Tube Cuff, a Class II (moderate risk) device regulated under 21 CFR 868.5800.