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FORCEPS FOR USE WITH RIGID ENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822193
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
32 days

FORCEPS FOR USE WITH RIGID ENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822193
510(k) Type
Traditional
Applicant
KELLEHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
32 days