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NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K942977
510(k) Type
Traditional
Applicant
NOVOSTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1995
Days to Decision
556 days
Submission Type
Summary

NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K942977
510(k) Type
Traditional
Applicant
NOVOSTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1995
Days to Decision
556 days
Submission Type
Summary