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MEDISYSTEMS PHERESIS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K862002
510(k) Type
Traditional
Applicant
MEDISYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1986
Days to Decision
35 days

MEDISYSTEMS PHERESIS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K862002
510(k) Type
Traditional
Applicant
MEDISYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1986
Days to Decision
35 days