Cleared Traditional

K790754 - BROWNE MODEL CF-1 AND CF-1G

K790754 is the FDA 510(k) clearance for BROWNE MODEL CF-1 AND CF-1G by Browne Corp.. It is a Class 2 Gastroenterology & Urology device (product code FAP) cleared through the Traditional 510(k) pathway after a 45-day FDA review.

K790754 · Browne Corp. · Gastroenterology & Urology device
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Jun 1979
Decision
45d
Days
Class 2
Risk

K790754 is an FDA 510(k) clearance for the BROWNE MODEL CF-1 AND CF-1G. Classified as Cystometric Gas (carbon-dioxide) On Hydraulic Device (product code FAP), Class II - Special Controls.

Submitted by Browne Corp. (Mchenry, US). The FDA issued a Cleared decision on June 1, 1979 after a review of 45 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1620 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Browne Corp. devices

Submission Details

510(k) Number K790754 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1979
Decision Date June 01, 1979
Days to Decision 45 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 130d · This submission: 45d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FAP Cystometric Gas (carbon-dioxide) On Hydraulic Device
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1620
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FAP Cystometric Gas (carbon-dioxide) On Hydraulic Device

All 25
Devices cleared under the same product code (FAP) and FDA review panel - the closest regulatory comparables to K790754.
UROCOMP REMOTE CONTROL 1804
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UROCOMP MODEL 1404
K821939 · Life-Tech Intl., Inc. · Jul 1982
ULTRALITE UROSYSTEM, MODELS GU-1 & GU-2
K790519 · American Medical Systems, Inc. · May 1979
UROFLOW-CYSTOMETER SYSTEM
K771850 · Richard Wolf Medical Instruments Corp. · Oct 1977