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VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000369
510(k) Type
Traditional
Applicant
MEDPRO TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2000
Days to Decision
55 days
Submission Type
Summary

VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000369
510(k) Type
Traditional
Applicant
MEDPRO TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2000
Days to Decision
55 days
Submission Type
Summary