EQL
8 FDA 510(k) clearances · Product code
72 daysmedian time to decision
86 days90th percentile
8clearances measured
FDA profile
- Official device name
- Laryngostroboscope
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4750
- Medical specialty
- Ear, Nose, Throat
- Adverse events (MAUDE)
- 2022: 32 · 2023: 25 · 2024: 39 · 2025: 29 · 2026: 14
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| RIWO DRIVE SYSTEM 2302 WITH GENERATOR, SMALL MOTOR HANDLES, 8563.111, 8563.351 (K984521) | Richard Wolf Medical Instruments Corp. | 1999-03-17 |
| 9105 RIGID TELESCOPIC ENDOSCOPE (K921285) | Kay Elemetrics Corp. | 1992-05-28 |
| RLS 9100 RHINO-LARYNGEAL STROBOSCOPE (K921184) | Kay Elemetrics Corp. | 1992-05-28 |
| ENDOSTROBOSCOPE IV (K884933) | Jedmed Instrument Co. | 1989-02-15 |
| RHINO-LARYNX STROBOSCOPE TYPE 4914 (K842090) | Bruel & Kjaer Industri A/S | 1984-07-18 |
| LARYNGOSTROBOSCOPE (K822523) | Kelleher Corp. | 1982-09-09 |
| PENTAX LARYNGO-STROBOSCOPE MODEL LS-1A (K801866) | Pentax Precision Instrument Corp. | 1980-09-16 |
| STOCKINGS, RVS TM (K770466) | Parke-Davis Co. | 1977-03-28 |
Track EQL automatically
Every clearance here is in the API, with alerts when new ones post.