Product code KYW— General Hospital
MEDICINE CUP
- Classification name
- Container, Liquid Medication, Graduated
- Device class
- Class 1
- Regulation
- 21 CFR 880.6430
- Advisory panel
- General Hospital
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code KYW
FDA has cleared devices under product code KYW between 1979 and 1980, filed by 2 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
- 1980
- 1979
Top applicants under product code KYW
Adverse events under product code KYW
product code KYW- Other
- 1
- Total
- 1
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 KYW
Data sourced from openFDA. This site is unofficial and independent of the FDA.