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LASEGUIDE CAT # CLF-600D & CLF-1000D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901786
510(k) Type
Traditional
Applicant
LASER PERIPHERALS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1990
Days to Decision
70 days

LASEGUIDE CAT # CLF-600D & CLF-1000D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901786
510(k) Type
Traditional
Applicant
LASER PERIPHERALS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1990
Days to Decision
70 days