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KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896183
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1990
Days to Decision
100 days

KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896183
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1990
Days to Decision
100 days