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KERR OPTIBOND, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934690
510(k) Type
Traditional
Applicant
KERR CORPORATION (DANBURY)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1993
Days to Decision
157 days
Submission Type
Summary

KERR OPTIBOND, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934690
510(k) Type
Traditional
Applicant
KERR CORPORATION (DANBURY)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1993
Days to Decision
157 days
Submission Type
Summary