The following data is part of a premarket notification filed by E-z-em, Inc. with the FDA for Sos Bloodless Needle.
| Device ID | K914330 |
| 510k Number | K914330 |
| Device Name: | SOS BLOODLESS NEEDLE |
| Classification | Introducer, Catheter |
| Applicant | E-Z-EM, INC. P.O. BOX 993 266 QUEENSBURY AVENUE Glens Falls, NY 12801 |
| Contact | Merribeth Adams |
| Correspondent | Merribeth Adams E-Z-EM, INC. P.O. BOX 993 266 QUEENSBURY AVENUE Glens Falls, NY 12801 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-27 |
| Decision Date | 1991-12-20 |