Disposable Inflation Gauge

FDA 510(k) K902695 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK902695

Submission

Device name
Disposable Inflation Gauge
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
June 19, 1990
Decision date
December 3, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
MAV – Syringe, Balloon Inflation
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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Questions and answers

When was Disposable Inflation Gauge cleared by the FDA?

Disposable Inflation Gauge (K902695) received a 510(k) decision of Substantially Equivalent on December 3, 1990, 167 days after the submission was received.

What is the product code of K902695?

The FDA product code is MAV – Syringe, Balloon Inflation, a Class II (moderate risk) device regulated under 21 CFR 870.1650.