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510(k) K841979

Device
4MM CUP CURRETTE
Applicant
STAINLESS MFG., INC.
510(k) number
K841979
Product code
HTF  
Decision
Substantially Equivalent (SESE)
Decision date
1984-06-19
Date received
1984-05-14
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#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

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
K890252BONE CURETTEKinetic Medical Products1989-01-27
K870778ACROMED WALLIE-HEINIG CURETTESBuckman Co., Inc.1987-03-09

Legacy Summary#

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FDA Review#

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