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510(k) K890389

Device
UMBILICAL SCISSORS
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890389
Product code
HDJ  
Decision
Substantially Equivalent (SESE)
Decision date
1989-02-13
Date received
1989-01-23
Regulation
884.4520
Classification name
Scissors, Umbilical
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JAMES I LAUGHNER
Address
4934 Peach St. Erie PA US 16509 16509

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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