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PALAXPRESS ULTRA POWDER (PINK); PALAXPRESS ULTRA LIQUID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110037
510(k) Type
Traditional
Applicant
HERAEUS KULZER, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2011
Days to Decision
113 days
Submission Type
Summary

PALAXPRESS ULTRA POWDER (PINK); PALAXPRESS ULTRA LIQUID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110037
510(k) Type
Traditional
Applicant
HERAEUS KULZER, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2011
Days to Decision
113 days
Submission Type
Summary