The following data is part of a premarket notification filed by Terumo Europe N.v. with the FDA for K-pack Ii Needle- 27g & 30g Thin Wall.
| Device ID | K110850 |
| 510k Number | K110850 |
| Device Name: | K-PACK II NEEDLE- 27G & 30G THIN WALL |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | TERUMO EUROPE N.V. INTERLEUVENLAAN 40 Leuven, BE 3001 |
| Contact | M.j. Aerts |
| Correspondent | M.j. Aerts TERUMO EUROPE N.V. INTERLEUVENLAAN 40 Leuven, BE 3001 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-03-28 |
| Decision Date | 2011-06-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 55413206223683 | K110850 | 000 |
| 55413206223645 | K110850 | 000 |
| 55413206211956 | K110850 | 000 |
| 55413206051040 | K110850 | 000 |
| 55413206051033 | K110850 | 000 |