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FDA 510(k)

BROWNE MODEL GD-5

K-Number: K792093 · 1979-12-06

ApplicantBrowne Corp.
Decision Date1979-12-06
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BROWNE MODEL GD-5 is the device name listed in this FDA 510(k) record. The listed applicant is Browne Corp.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792093. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROWNE MODEL GD-5?

BROWNE MODEL GD-5 is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Browne Corp.. The 510(k) number is K792093.

When did BROWNE MODEL GD-5 receive FDA 510(k) clearance?

BROWNE MODEL GD-5 received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792093.

Who is the listed applicant for BROWNE MODEL GD-5?

The FDA 510(k) record lists Browne Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BROWNE MODEL GD-5?

The FDA product code for BROWNE MODEL GD-5 is FAP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Browne Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K792091BROWNE MODEL UD-4DK792090BROWNE MODEL UD-4K792092BROWNE MODEL UD-4EK792094BROWNE MODEL UA-6K790478BROWNE MODEL UD-4DEK790754BROWNE MODEL CF-1 AND CF-1G

View all 7 devices →

Related Devices (Code: FAP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113771SIGNAL GEAR URETHRAL CATHETER ELECTRODENeurovision Medical Products, Inc.K974775SINGLE CHANNEL UROLOGICAL PRESSURE GAUGE, DUAL CHANNEL UROLOGICAL PRESSURE GAUGEAirtronic Services, Inc.K963330URODYNAMIC ANALYSIS MODULESynectics Medical, Inc.K962472RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETERRusch Intl.K931175SCHUSTER DISPOSABLE BALLOON PROBESandhill Scientific, Inc.K931179UROLAB SPECTRUMLife-Tech Intl., Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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