K072482 is an FDA 510(k) clearance for the HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY. This device is classified as a Syringe, Antistick (Class II - Special Controls, product code MEG).
Submitted by Smiths Medical Asd, Inc. (Keene, US). The FDA issued a Cleared decision on November 29, 2007, 86 days after receiving the submission on September 4, 2007.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5860.
| 510(k) Number | K072482 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 04, 2007 |
| Decision Date | November 29, 2007 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | MEG — Syringe, Antistick |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 880.5860 |