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FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872350
510(k) Type
Traditional
Applicant
LASER MEDIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1987
Days to Decision
54 days

FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872350
510(k) Type
Traditional
Applicant
LASER MEDIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1987
Days to Decision
54 days