Product code MOQ— General, Plastic Surgery
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822
- Classification name
- Battery, Replacement, Rechargeable
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code MOQ
FDA has cleared devices under product code MOQ between 1998 and 2008, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2008
- 2001
- 1998
Top applicants under product code MOQ
Adverse events under product code MOQ
product code MOQ- Malfunction
- 1,643
- Total
- 1,643
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code MOQ
Data sourced from openFDA. This site is unofficial and independent of the FDA.