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INDURENT GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935892
510(k) Type
Traditional
Applicant
ZHERMACK DENTAL PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1995
Days to Decision
735 days
Submission Type
Statement

INDURENT GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935892
510(k) Type
Traditional
Applicant
ZHERMACK DENTAL PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1995
Days to Decision
735 days
Submission Type
Statement