Last synced on 25 January 2026 at 3:41 am

ENT CHISELS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822165
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
24 days

ENT CHISELS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822165
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
24 days