DeviceClearance

Product code DWZ— Cardiovascular

BIOPSY FORCEPS

Classification name
Device, Biopsy, Endomyocardial
Device class
Class 2
Regulation
21 CFR 870.4075
Advisory panel
Cardiovascular
Total cleared
23
First cleared
Most recent

Market context for product code DWZ

FDA has cleared 23 devices under product code DWZ between 1981 and 2025, filed by 16 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 DWZ

Recent clearances under product code DWZ

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