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HEMORRELIEF DEVICE

Page Type
Cleared 510(K)
510(k) Number
K973590
510(k) Type
Traditional
Applicant
A.Stein - Regulatory Affairs Consulting
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/5/1998
Days to Decision
136 days
Submission Type
Statement

HEMORRELIEF DEVICE

Page Type
Cleared 510(K)
510(k) Number
K973590
510(k) Type
Traditional
Applicant
A.Stein - Regulatory Affairs Consulting
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/5/1998
Days to Decision
136 days
Submission Type
Statement