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510(k) K890252

Device
BONE CURETTE
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890252
Product code
HTF  
Decision
Substantially Equivalent (SESE)
Decision date
1989-01-27
Date received
1989-01-18
Regulation
878.4800
Classification name
Curette
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
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 HTF  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K870778ACROMED WALLIE-HEINIG CURETTESBuckman Co., Inc.1987-03-09
K8419794MM CUP CURRETTEStainless Mfg., Inc.1984-06-19

Legacy Summary#

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FDA Review#

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