BSF
8 FDA 510(k) clearances · Product code
53 daysmedian time to decision
168 days90th percentile
8clearances measured
FDA profile
- Official device name
- Absorber, Carbon-Dioxide
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5310
- Medical specialty
- Anesthesiology
- Adverse events (MAUDE)
- 2004: 5 · 2005: 2 · 2006: 23 · 2007: 2 · 2008: 3 · 2009: 4
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 |
|---|---|---|
| KAB SYSTEM (K951093) | King Systems Corp. | 1995-03-24 |
| OHMEDA GMS ABOSORBER (K852071) | Ohmeda Medical | 1985-07-15 |
| OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOR (K843422) | Ohmeda Medical | 1984-10-23 |
| NITROUS OXIDE RECYCLER (K834535) | G & L Unltd. | 1984-06-07 |
| OHIO GMS ABSORBER (K833452) | Airco/Ohio Medical Products | 1983-11-29 |
| OHIO ABSORBER (K821144) | Ohio Medical Products | 1982-05-28 |
| PENLON JUMBO CARBON DIOXIDE ABSORBER (K801255) | Penlon, Inc. | 1980-06-04 |
| ABSORBER, ANESTHESIA CIRCLE SYS, CO2 (K760076) | Fraser Sweatman, Inc. | 1976-07-16 |
Track BSF automatically
Every clearance here is in the API, with alerts when new ones post.