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KELOCOTE SCAR GEL AND KELOCOTE LASER GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973572
510(k) Type
Traditional
Applicant
HANSON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1997
Days to Decision
32 days
Submission Type
Summary

KELOCOTE SCAR GEL AND KELOCOTE LASER GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973572
510(k) Type
Traditional
Applicant
HANSON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1997
Days to Decision
32 days
Submission Type
Summary