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510(k) K760172

Device
OBTURATOR, VISUAL
Applicant
V. MUELLER O.V. BAXTER HEALTHCARE CORP.
510(k) number
K760172
Product code
FEC  
Decision
Substantially Equivalent (SESE)
Decision date
1976-12-02
Date received
1976-07-06
Regulation
876.1500
Classification name
Obturator, For Endoscope
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 FEC  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K001328INTRODUCER SHEATHNovasys Medical, Inc.2000-07-17
K760183OBTURATOR, DEFLECTINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-02

Legacy Summary#

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FDA Review#

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