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NEXUS BIOWAVE 7W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 10W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 30W PRO IR LAMP SYSTEM, NEXUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101893
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2011
Days to Decision
225 days
Submission Type
Summary

NEXUS BIOWAVE 7W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 10W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 30W PRO IR LAMP SYSTEM, NEXUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101893
510(k) Type
Traditional
Applicant
USA LASER BIOTECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2011
Days to Decision
225 days
Submission Type
Summary