Product code HFW— Obstetrics/Gynecology

UMBILICAL CORD CLAMP

Classification name
Clamp, Umbilical
Device class
Class 2
Regulation
21 CFR 884.4530
Advisory panel
Obstetrics/Gynecology
Total cleared
36
First cleared
Most recent

Market context for product code HFW

FDA has cleared 36 devices under product code HFW between 1978 and 2004, filed by 30 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code HFW

Recent clearances under product code HFW

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