The following data is part of a premarket notification filed by Jensen Industries, Inc. with the FDA for Willi Geller Creation And Lf Porcelain.
| Device ID | K002904 |
| 510k Number | K002904 |
| Device Name: | WILLI GELLER CREATION AND LF PORCELAIN |
| Classification | Powder, Porcelain |
| Applicant | JENSEN INDUSTRIES, INC. 50 STILLMAN RD. North Haven, CT 06473 |
| Contact | John Slanski |
| Correspondent | John Slanski JENSEN INDUSTRIES, INC. 50 STILLMAN RD. North Haven, CT 06473 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-09-18 |
| Decision Date | 2000-11-06 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| ECWG3022521 | K002904 | 000 |
| ECWG3022231 | K002904 | 000 |
| ECWG3021561 | K002904 | 000 |
| ECWG3021511 | K002904 | 000 |
| ECWG3020591 | K002904 | 000 |
| ECWG3020581 | K002904 | 000 |
| ECWG3020521 | K002904 | 000 |
| ECWG3020321 | K002904 | 000 |