Product code KXG— General Hospital
PROFILE SWAB CAT.#5273 & 5274
- Classification name
- Applicator, Absorbent Tipped, Sterile
- Device class
- Class 1
- Regulation
- 21 CFR 880.6025
- Advisory panel
- General Hospital
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KXG
FDA has cleared device under product code KXG, all in 1980, filed by 1 applicant company. 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.
Top applicants under product code KXG
Adverse events under product code KXG
product code KXG- Injury
- 290
- Total
- 290
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 KXG
Data sourced from openFDA. This site is unofficial and independent of the FDA.