FDA 510(k) Applications Submitted by ENTER MEDICAL CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K042556 | 09/20/2004 | SHINEBALL PVC MANUAL RESUSCIATOR, ENT-1001, ENT-1003, ENT-1005, SHINEBALL SILICONE MANUAL RESUSCIATOR, ENT-1022, | ENTER MEDICAL CORPORATION |
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