Last synced on 19 July 2024 at 11:05 pm

MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880930
510(k) Type
Traditional
Applicant
COPPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1988
Days to Decision
88 days

MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880930
510(k) Type
Traditional
Applicant
COPPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1988
Days to Decision
88 days