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FDA 510(k) Applications Submitted by ROCAP DIV. OF SABRATEK CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990308
02/01/1999
ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML
ROCAP DIV. OF SABRATEK CORP.
K990390
02/09/1999
HEPARIN IV FLUSH SYRINGE, 10 U/ML \
ROCAP DIV. OF SABRATEK CORP.
K984614
12/29/1998
NORMAL SALINE FLUSH SYRINGE
ROCAP DIV. OF SABRATEK CORP.
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