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HYBRID SURGICAL DEVICES, MODIFICIATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951353
510(k) Type
Traditional
Applicant
LASER CENTERS OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1995
Days to Decision
38 days
Submission Type
Statement

HYBRID SURGICAL DEVICES, MODIFICIATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951353
510(k) Type
Traditional
Applicant
LASER CENTERS OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1995
Days to Decision
38 days
Submission Type
Statement