Product code DPT— Cardiovascular

A-V RECORDER

Classification name
Probe, Blood-Flow, Extravascular
Device class
Class 2
Regulation
21 CFR 870.2120
Advisory panel
Cardiovascular
Total cleared
48
First cleared
Most recent

Market context for product code DPT

FDA has cleared 48 devices under product code DPT between 1978 and 2024, filed by 33 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 DPT

Recent clearances under product code DPT

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