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NORMAL SALINE FLUSH SYRINGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984614
510(k) Type
Traditional
Applicant
Rocap Div. of Sabratek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1999
Days to Decision
149 days
Submission Type
Statement

NORMAL SALINE FLUSH SYRINGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984614
510(k) Type
Traditional
Applicant
Rocap Div. of Sabratek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1999
Days to Decision
149 days
Submission Type
Statement