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510(k) K930034

Device
CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON
Applicant
THOMASVILLE MEDICAL ASSOC.
510(k) number
K930034
Product code
HDQ  
Decision
Substantially Equivalent (SESE)
Decision date
1994-02-24
Date received
1993-01-05
Regulation
884.4530
Classification name
Dilator, Cervical, Fixed Size
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
THOMAS J ZINNANTI
Address
935 Cobblestone Ct. Alpharetta GA US 30201 30201

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HDQ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K896701TEFLON CERVICAL ACCESS SETCook Ob/Gyn1990-09-13
K891029CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALLZinnanti Surgical Instruments, Inc.1989-03-17
K890377FIXED-SIZE UTERINE DILATORKinetic Medical Products1989-02-13
K811568CERVICAL DILATORGynemetrics, Inc.1981-07-16
K791277MODEL 6500 EXTRACTION IRRIGATION SYSCavitron Corp.1979-08-22

Legacy Summary#

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FDA Review#

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