Last synced on 25 April 2025 at 11:05 pm

COHERENT POPEYE OPHTHALMIC LASER SYSTEM, COHERENT POPEYE OPHTHALMIC LASER SYSTEM IN COMBINATION WITH THE COHERENT ARGONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973470
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1997
Days to Decision
88 days
Submission Type
Summary

COHERENT POPEYE OPHTHALMIC LASER SYSTEM, COHERENT POPEYE OPHTHALMIC LASER SYSTEM IN COMBINATION WITH THE COHERENT ARGONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973470
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1997
Days to Decision
88 days
Submission Type
Summary