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GENTLERAY 980 DIODE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072262
510(k) Type
Traditional
Applicant
KAVO AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2007
Days to Decision
72 days
Submission Type
Summary

GENTLERAY 980 DIODE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072262
510(k) Type
Traditional
Applicant
KAVO AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2007
Days to Decision
72 days
Submission Type
Summary