CBL
5 FDA 510(k) clearances · Product code
64 daysmedian time to decision
183 days90th percentile
5clearances measured
FDA profile
- Official device name
- Absorbent, Carbon-Dioxide
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5300
- Medical specialty
- Anesthesiology
- Adverse events (MAUDE)
- 2008: 3 · 2009: 2 · 2010: 8 · 2021: 22 · 2022: 20 · 2025: 17
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 |
|---|---|---|
| SOFNOLIME CARBON DIOXIDE ABSORBENT (K921803) | Molecular Products , Ltd. | 1992-10-15 |
| DISPOSABLE CO2 ABSORBER/E (K897171) | Gibeck, Inc. | 1990-03-13 |
| CARBON DIOXIDE ABSORBENTS (K860147) | Dentsply Intl. | 1986-02-28 |
| MEDIPART SODA LIME MP-3522 (K853571) | Medipart Jerry Alexander | 1985-10-29 |
| BARALYME CO2 ABSORBENT (K811260) | Allied Healthcare Products, Inc. | 1981-05-27 |
Track CBL automatically
Every clearance here is in the API, with alerts when new ones post.