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MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST 200)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091323
510(k) Type
Special
Applicant
INTERMEDIC ARFRAN, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2009
Days to Decision
30 days
Submission Type
Summary

MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST 200)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091323
510(k) Type
Special
Applicant
INTERMEDIC ARFRAN, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2009
Days to Decision
30 days
Submission Type
Summary