FDA.reportPublic FDA data

510(k) K870778

Device
ACROMED WALLIE-HEINIG CURETTES
Applicant
BUCKMAN CO., INC.
510(k) number
K870778
Product code
HTF  
Decision
Substantially Equivalent (SESE)
Decision date
1987-03-09
Date received
1987-02-26
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
DAVID W SCHLERF
Address
921 Calle Verde Martinez CA US 94553 94553

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
K8419794MM CUP CURRETTEStainless Mfg., Inc.1984-06-19

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases