Last synced on 25 January 2026 at 3:41 am

LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIOLASE FOR LASERENAP)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983524
510(k) Type
Traditional
Applicant
Lares Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1999
Days to Decision
175 days
Submission Type
Statement

LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIOLASE FOR LASERENAP)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983524
510(k) Type
Traditional
Applicant
Lares Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1999
Days to Decision
175 days
Submission Type
Statement