FDA 510(k) Applications Submitted by PHYSICIAN INDUSTRIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960248 | 01/16/1996 | GENERAL PROCEDURE KIT | PHYSICIAN INDUSTRIES, INC. |
| K040565 | 03/03/2004 | PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE | PHYSICIAN INDUSTRIES, INC. |
| K033739 | 11/28/2003 | PHYSICIAN INDUSTRIES' DURAMETER SYRINGE | PHYSICIAN INDUSTRIES, INC. |
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