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LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCKETPRO OR POCKETPRO S4)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011960
510(k) Type
Traditional
Applicant
LARES RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
182 days
Submission Type
Summary

LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCKETPRO OR POCKETPRO S4)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011960
510(k) Type
Traditional
Applicant
LARES RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
182 days
Submission Type
Summary