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PHERESIS NEEDLE ASSEMBLY

Page Type
Cleared 510(K)
510(k) Number
K810076
510(k) Type
Traditional
Applicant
HAEMONETICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1981
Days to Decision
51 days

PHERESIS NEEDLE ASSEMBLY

Page Type
Cleared 510(K)
510(k) Number
K810076
510(k) Type
Traditional
Applicant
HAEMONETICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1981
Days to Decision
51 days