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SHARPLAN 1041 SEALED-OFF CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900077
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
61 days

SHARPLAN 1041 SEALED-OFF CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900077
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
61 days