The following data is part of a premarket notification filed by Arrow Intl., Inc. with the FDA for Non-coring Needle.
| Device ID | K961088 |
| 510k Number | K961088 |
| Device Name: | NON-CORING NEEDLE |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | ARROW INTL., INC. 1600 PROVIDENCE HIGHWAY Walpole, MA 02081 |
| Contact | Richard J Clark |
| Correspondent | Richard J Clark ARROW INTL., INC. 1600 PROVIDENCE HIGHWAY Walpole, MA 02081 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-19 |
| Decision Date | 1996-07-02 |