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510(k) K890221

Device
MICROSURGICAL WIRE LOOP
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890221
Product code
JYQ  
Decision
Substantially Equivalent (SESE)
Decision date
1989-01-27
Date received
1989-01-18
Regulation
874.4420
Classification name
Loop, Wire
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
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

Other 510(k) Records For Product Code JYQ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K870761EAR LOOPTreace Medical, Inc.1987-03-03

Legacy Summary#

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FDA Review#

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