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MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912265
510(k) Type
Traditional
Applicant
MEDICAL LASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1991
Days to Decision
141 days
Submission Type
Statement

MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912265
510(k) Type
Traditional
Applicant
MEDICAL LASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1991
Days to Decision
141 days
Submission Type
Statement