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MODIFIED CO2 ND:YAG LASER MODEL 880, OB-GYN APPLI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871220
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1987
Days to Decision
118 days

MODIFIED CO2 ND:YAG LASER MODEL 880, OB-GYN APPLI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871220
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1987
Days to Decision
118 days