The following data is part of a premarket notification filed by Minrad, Inc. with the FDA for Light Saber Aspiration Needle.
| Device ID | K982018 |
| 510k Number | K982018 |
| Device Name: | LIGHT SABER ASPIRATION NEEDLE |
| Classification | Syringe, Piston |
| Applicant | MINRAD, INC. 6576 EAST QUAKER ST. Orchard Park, NY 14127 -2593 |
| Contact | John Mcneirney |
| Correspondent | John Mcneirney MINRAD, INC. 6576 EAST QUAKER ST. Orchard Park, NY 14127 -2593 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-06-08 |
| Decision Date | 1998-08-07 |