FDA 510(k) Applications Submitted by ERROL SINGH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090262 | 02/03/2009 | PERCUCATH URINARY CATHETER | PERCUVISION LLC |
| K091600 | 06/03/2009 | DIRECTVISION GUIDE SYSTEM | PERCUVISION LLC |
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