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ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE

Page Type
Cleared 510(K)
510(k) Number
K062399
510(k) Type
Traditional
Applicant
ROCKWELL MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2006
Days to Decision
93 days
Submission Type
Summary

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE

Page Type
Cleared 510(K)
510(k) Number
K062399
510(k) Type
Traditional
Applicant
ROCKWELL MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2006
Days to Decision
93 days
Submission Type
Summary