Submission Details
| 510(k) Number | K251500 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 15, 2025 |
| Decision Date | June 09, 2025 |
| Days to Decision | 25 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K251500 is an FDA 510(k) clearance for the MallyaG Injection Pen Adapter (MallyaG), a Injection Data Capture Device (Class II — Special Controls, product code QOG), submitted by Biocorp Production (Issoire, FR). The FDA issued a Cleared decision on June 9, 2025, 25 days after receiving the submission on May 15, 2025. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5860.
| 510(k) Number | K251500 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 15, 2025 |
| Decision Date | June 09, 2025 |
| Days to Decision | 25 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | QOG — Injection Data Capture Device |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 880.5860 |
| Definition | An Injection Data Capture Device Is An Electrically-powered/electromechanical Accessory That Interfaces With Reusable Or Disposable Injection Devices For The Purposes Of Interpreting, Recording And Displaying And/or Transmitting Injection Data To A Connected Application Or Software. |