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510(k) K822196

Device
EAR SCISSORS
Applicant
KELLEHER CORP.
510(k) number
K822196
Product code
JZB  
Decision
Substantially Equivalent (SESE)
Decision date
1982-08-30
Date received
1982-07-23
Regulation
874.4420
Classification name
Scissors, Ear
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
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 JZB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K914226ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACKE.I. Dupont DE Nemours & Co., Inc.1991-11-19
K870756VEIN GRAFT EAR SCISSORSTreace Medical, Inc.1987-03-03
K833603SCISSORS SHEA BELLUCCMicrotek Medical, Inc.1984-01-03

Legacy Summary#

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FDA Review#

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