MPA
- Product code
- MPA
- Device name
- Endoilluminator
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 41 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253468 | 2026-08-10 | Nova Eye, Inc. | Nova Eye iTrack 250A Canaloplasty Microcatheter (iT… | |
| K242184 | 2024-12-04 | Alcon Laboratories, Inc. | Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wid… | |
| K233653 | 2024-08-05 | Peregrine Surgical, LLC | Midfield Light Pipe, 23ga (3269.M06-00); Midfield Li… |
Official FDA classification page: MPA
Classification and pathway per current FDA publications. Data from openFDA (CC0).