The following data is part of a premarket notification filed by Pmt Corp. with the FDA for Pmt Sphenoidal Electrode And Accessory, Model 2101-31 And 2102-31 Series.
| Device ID | K033730 |
| 510k Number | K033730 |
| Device Name: | PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIES |
| Classification | Electrode, Depth |
| Applicant | PMT CORP. 1500 PARK RD. Chanhassen, MN 55317 |
| Contact | Eric Caille |
| Correspondent | Eric Caille PMT CORP. 1500 PARK RD. Chanhassen, MN 55317 |
| Product Code | GZL |
| CFR Regulation Number | 882.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-11-28 |
| Decision Date | 2004-08-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00650551092988 | K033730 | 000 |
| 10650551092954 | K033730 | 000 |
| 10650551092930 | K033730 | 000 |
| 10650551092916 | K033730 | 000 |
| 10650551092893 | K033730 | 000 |
| 10650551092879 | K033730 | 000 |
| 10650551092862 | K033730 | 000 |
| 10650551092855 | K033730 | 000 |
| 10650551092848 | K033730 | 000 |
| 10650551092831 | K033730 | 000 |
| 10650551092824 | K033730 | 000 |
| 10650551092817 | K033730 | 000 |
| 10650551092961 | K033730 | 000 |
| 10650551092992 | K033730 | 000 |
| 10650551092732 | K033730 | 000 |
| 00650551092971 | K033730 | 000 |
| 10650551092947 | K033730 | 000 |
| 10650551092923 | K033730 | 000 |
| 10650551092909 | K033730 | 000 |
| 10650551092886 | K033730 | 000 |
| 00650551092797 | K033730 | 000 |
| 00650551092780 | K033730 | 000 |
| 00650551092773 | K033730 | 000 |
| 10650551092763 | K033730 | 000 |
| 10650551092756 | K033730 | 000 |
| 10650551092749 | K033730 | 000 |
| 10650551092800 | K033730 | 000 |