510(k) K760174

Device
ADAPTER, RESECTOSCOPE
Applicant
V. MUELLER O.V. BAXTER HEALTHCARE CORP.
510(k) number
K760174
Product code
FDC  
Decision
Substantially Equivalent (SESE)
Decision date
1976-08-30
Date received
1976-07-06
Regulation
876.1500
Classification name
Resectoscope, Working Element
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FDC  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K021166ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BRAcmi-Circon Corporation2002-05-09
K992141OLYMPUS WORKING ELEMENT FOR PROBESOlympus Winter & Ibe GmbH1999-09-29
K991426MAHE INSTRUMENTSMahe Intl., Inc.1999-08-05
K942626CONTINUOUS FLOW BIOPSY PROBEGm Engineering, Inc.1995-05-30
K933962GM CONTINUOUS FLOW BIOPSY PROBEGm Engineering, Inc.1994-02-25
K895643MODIFIED UROPUMP* FLUID MANAGEMENT SYSTEMOrthoconcept, Inc.1989-10-17
K894363UROPUMP* FLUID MANAGEMENT SYSTEMOrthoconcept, Inc.1989-08-11
K842997LASER RECTOSCOPE SET 784Laser Industries , Ltd.1984-08-27
K760182SHEATH, RESECTOSCOPEV. Mueller O.V. Baxter Healthcare Corp.1976-12-02
K760184ELEMENT, WORKINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-02

Legacy Summary#

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FDA Review#

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