The following data is part of a premarket notification filed by Lily Imaging Solutions Co. with the FDA for Lily Multicannula Guide.
| Device ID | K954999 |
| 510k Number | K954999 |
| Device Name: | LILY MULTICANNULA GUIDE |
| Classification | Instrument, Biopsy |
| Applicant | LILY IMAGING SOLUTIONS CO. 1966 LOOP RD. Fortuna, CA 95540 |
| Contact | Gary H Baker |
| Correspondent | Gary H Baker LILY IMAGING SOLUTIONS CO. 1966 LOOP RD. Fortuna, CA 95540 |
| Product Code | KNW |
| CFR Regulation Number | 876.1075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-01 |
| Decision Date | 1996-04-04 |