Product code GAB— General, Plastic Surgery
ANCHOR BRAND SURGICAL NEEDLES
- Classification name
- Needle, Suturing, Disposable
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 8
- First cleared
- Most recent
Market context for product code GAB
FDA has cleared devices under product code GAB between 1980 and 2001, filed by 8 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
- 2001
- 1998
- 1993
- 1989
- 1986
- 1983
- 1981
- 1980
Top applicants under product code GAB
Recent clearances under product code GAB
- K012199 — DIGICAP
- K980988 — AXYA MEDICAL, INC. AUTOMATIC SUTURING AND LIGATING SYSTEM-(ASLS)
- K932591 — ENDO-JUDGE
- K895681 — CONTRAST BACKGROUND MATERIAL
- K863595 — COATED SUTURE NEEDLE
- K831648 — ANCHOR BRAND SURGICAL NEEDLES
- K812444 — RADIATION STERILIZATION FOR NEEDLE CNTR
- K801976 — SCANLAN STERNUM NEEDLE-SUTURE
Data sourced from openFDA. This site is unofficial and independent of the FDA.