MRB
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Indicator, Biological, Liquid Chemical Sterilization Process
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.2800
- Medical specialty
- General Hospital
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SPSMEDICAL SPORVIEW PA CULTURE SET (K081879) | Spsmedical Supply Corp. | 2008-07-30 |
| RAVEN PROPACT (K053212) | Raven Biological Laboratories, Inc. | 2006-02-15 |
| SPSMEDICAL SPORVIEW PA CULTURE SET (K043135) | Spsmedical Supply Corp. | 2005-01-13 |
| PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA (K031114) | Raven Biological Laboratories, Inc. | 2004-03-03 |
Track MRB automatically
Every clearance here is in the API, with alerts when new ones post.