Product code FZS— General, Plastic Surgery
ACU-CURETTE
- Classification name
- Curette, Surgical, General Use
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 14
- First cleared
- Most recent
Market context for product code FZS
FDA has cleared devices under product code FZS between 1981 and 1994, filed by 13 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
- 1994
- 1990
- 1989
- 1988
- 1987
- 1985
- 1984
- 1983
- 1981
Top applicants under product code FZS
Recent clearances under product code FZS
- K932493 — SURGICAL CURETTE
- K902000 — KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD
- K892521 — CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE
- K891888 — CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER
- K891334 — ACU-CURETTE
- K890366 — ADENOID CURETTE
- K875292 — MICRODISCECTOMY CURETTE SET
- K871925 — STRAIGHT CUP CURRETTE, 1.7MM
- K854888 — RANDALL CURETTE
- K854899 — NOVAK CURETTE
- K842701 — HOPPENSTEIN MICROSURGICAL SPINAL INSTRU
- K831367 — PMN VOLZ CURETTES
- K831119 — LUO CURRETTES #3211
- K803178 — ANSPACH MENISECTOMY KNIFE
Data sourced from openFDA. This site is unofficial and independent of the FDA.