Product code BRY— Anesthesiology
ANESTHASSIST
- Classification name
- Cabinet, Table And Tray, Anesthesia
- Device class
- Class 1
- Regulation
- 21 CFR 868.6100
- Advisory panel
- Anesthesiology
- Total cleared
- 5
- First cleared
- Most recent
Market context for product code BRY
FDA has cleared devices under product code BRY between 1982 and 1992, filed by 5 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
- 1992
- 1991
- 1990
- 1987
- 1982
Top applicants under product code BRY
Adverse events under product code BRY
product code BRY- Death
- 9
- Malfunction
- 75,890
- Total
- 75,899
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 BRY
Data sourced from openFDA. This site is unofficial and independent of the FDA.