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MODIFIED FORMED-EXTENSION MAHURKAR DUAL LUMEN CATH

Page Type
Cleared 510(K)
510(k) Number
K880583
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1988
Days to Decision
13 days

MODIFIED FORMED-EXTENSION MAHURKAR DUAL LUMEN CATH

Page Type
Cleared 510(K)
510(k) Number
K880583
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1988
Days to Decision
13 days