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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