Klein Rectal Tampnade Balloon

FDA 510(k) K933842 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK933842

Submission

Device name
Klein Rectal Tampnade Balloon
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
August 6, 1993
Decision date
September 29, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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Questions and answers

When was Klein Rectal Tampnade Balloon cleared by the FDA?

Klein Rectal Tampnade Balloon (K933842) received a 510(k) decision of Substantially Equivalent on September 29, 1994, 419 days after the submission was received.

What is the product code of K933842?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.