Tracheostomy Care Kit (Sterile)

FDA 510(k) K925020 · Customed, Inc.

Unknown

510(k) numberK925020

Submission

Device name
Tracheostomy Care Kit (Sterile)
Applicant
Customed, Inc.
Fajardo, PR, US
Received
September 24, 1992
Decision date
July 7, 1993
Decision
Unknown (SESK)
Type
Traditional 510(k)
Summary
510(k) statement 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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Questions and answers

When was Tracheostomy Care Kit (Sterile) cleared by the FDA?

Tracheostomy Care Kit (Sterile) (K925020) received a 510(k) decision of Unknown on July 7, 1993, 286 days after the submission was received.

What is the product code of K925020?

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