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HEPARIN IV FLUSH SYRINGE, 10 U/ML \

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990390
510(k) Type
Traditional
Applicant
Rocap Div. of Sabratek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1999
Days to Decision
304 days
Submission Type
Statement

HEPARIN IV FLUSH SYRINGE, 10 U/ML \

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990390
510(k) Type
Traditional
Applicant
Rocap Div. of Sabratek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1999
Days to Decision
304 days
Submission Type
Statement