The following data is part of a premarket notification filed by Medline Industries, Inc. with the FDA for Medline Syringes, Multiple.
| Device ID | K061275 |
| 510k Number | K061275 |
| Device Name: | MEDLINE SYRINGES, MULTIPLE |
| Classification | Syringe, Piston |
| Applicant | MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundelein, IL 60060 |
| Contact | Lara N Simmons |
| Correspondent | Lara N Simmons MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundelein, IL 60060 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-05-08 |
| Decision Date | 2006-07-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40888277804914 | K061275 | 000 |
| 40888277804983 | K061275 | 000 |
| 40889942172277 | K061275 | 000 |
| 10195327614775 | K061275 | 000 |
| 10195327614676 | K061275 | 000 |