FDA.reportPublic FDA data

510(k) K890225

Device
SURGICAL SCISSORS
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890225
Product code
HRR  
Decision
Substantially Equivalent (SESE)
Decision date
1989-01-27
Date received
1989-01-18
Regulation
888.4540
Classification name
Scissors, Orthopedic, Surgical
Medical specialty
Orthopedic
Review panel
Orthopedic
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 HRR  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K890212MICROSURGICAL SCISSORSKinetic Medical Products1989-01-27
K890261TRIGEMINAL SCISSORSKinetic Medical Products1989-01-27
K873501SCISSOR, LEFTArthropedics, Inc.1987-11-02
K873502SCISSOR, RIGHTArthropedics, Inc.1987-11-02
K85180069-100 TO 69-114 VARIOUS CUTICLE SCISSORSArtiberia1985-06-20
K842953ALL-HANDS MEDICAL SUPPLY SUTURE REMOVALAll-Hands Medical Supply, Inc.1984-08-21
K800721GENERAL UTILITY SURG. SCISSORS #460180-Edward Weck, Inc.1980-05-08

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