DeviceClearance

Product code HTF— General, Plastic Surgery

4MM CUP CURRETTE

Classification name
Curette
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
3
First cleared
Most recent

Market context for product code HTF

FDA has cleared 3 devices under product code HTF between 1984 and 1989, 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

Top applicants under product code HTF

Adverse events under product code HTF

product code HTF
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 HTF

Data sourced from openFDA. This site is unofficial and independent of the FDA.