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MCL 29 DERMABLATE ER:YAG LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992707
510(k) Type
Traditional
Applicant
Aesculap-Meditec North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1999
Days to Decision
69 days
Submission Type
Summary

MCL 29 DERMABLATE ER:YAG LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992707
510(k) Type
Traditional
Applicant
Aesculap-Meditec North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1999
Days to Decision
69 days
Submission Type
Summary