Product code MRB— General Hospital
SPSMEDICAL SPORVIEW PA CULTURE SET
- Classification name
- Indicator, Biological, Liquid Chemical Sterilization Process
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code MRB
FDA has cleared devices under product code MRB between 2004 and 2008, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2008
- 2006
- 2005
- 2004
Top applicants under product code MRB
Recent clearances under product code MRB
Data sourced from openFDA. This site is unofficial and independent of the FDA.