Cleared Traditional

K902695 - DISPOSABLE INFLATION GAUGE

K902695 is an FDA 510(k) clearance for DISPOSABLE INFLATION GAUGE, manufactured by Cook Urological, Inc.. The device is a Class 2 Cardiovascular device with product code MAV cleared through the Traditional 510(k) pathway after a 167-day FDA review.

K902695 · Cook Urological, Inc. · Cardiovascular device
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Dec 1990
Decision
167d
Days
Class 2
Risk

K902695 is an FDA 510(k) clearance for the DISPOSABLE INFLATION GAUGE. Classified as Syringe, Balloon Inflation (product code MAV), Class II - Special Controls.

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on December 3, 1990 after a review of 167 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1650 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Cook Urological, Inc. devices

FDA 510(k) Submission Details - K902695

510(k) Number K902695 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 19, 1990
Decision Date December 03, 1990
Days to Decision 167 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d slower than avg
Panel avg: 125d · This submission: 167d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MAV Device Classification - Class 2, Special Controls

Product Code MAV Syringe, Balloon Inflation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1650
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - MAV Syringe, Balloon Inflation

All 42
Devices cleared under the same product code (MAV) and FDA review panel - the closest regulatory comparables to K902695.
CONDOR ANALOG INFLATION SYRINGE
K904508 · Professional Medical Services · Apr 1991
CONDOR DIGITAL INFLATION SYRINGE
K904954 · Professional Medical Services · Jan 1991
MORSE BALLOON INFLATION DEVICE
K904275 · North American Instrument Corp. · Jan 1991
INFLATION/DEFLATION DEVICE
K904394 · Boston Scientific Corp · Dec 1990
CATHETER BALLOON DILATOR PRESSURE GAUGE
K895511 · Argon Medical Corp. · Feb 1990
ACS INDEFLATOR XX
K896849 · Advanced Cardiovascular Systems, Inc. · Feb 1990