510(k) K041094

Device
HSG CATHETER SET
Applicant
Bioteque America, Inc.
510(k) number
K041094
Product code
LKF
Decision
Substantially Equivalent (SESE)
Decision date
2004-06-17
Date received
2004-04-27
Regulation
884.4530
Classification name
Cannula, Manipulator/Injector, Uterine
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
DENIS DORSEY
Address
340 E. Maple Ave., #204-C Langhorne PA US 19047 19047

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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