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CONTINUOUS FLUSH DEVICE/FDI

Page Type
Cleared 510(K)
510(k) Number
K820202
510(k) Type
Traditional
Applicant
LINTON BIOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1982
Days to Decision
17 days

CONTINUOUS FLUSH DEVICE/FDI

Page Type
Cleared 510(K)
510(k) Number
K820202
510(k) Type
Traditional
Applicant
LINTON BIOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1982
Days to Decision
17 days