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NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091726
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2009
Days to Decision
139 days
Submission Type
Summary

NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091726
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2009
Days to Decision
139 days
Submission Type
Summary