DeviceClearance

Product code DSA— Cardiovascular

PATIENT CABLE

Classification name
Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class 2
Regulation
21 CFR 870.2900
Advisory panel
Cardiovascular
Total cleared
105
First cleared
Most recent

Market context for product code DSA

FDA has cleared 105 devices under product code DSA between 1977 and 2026, filed by 78 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 DSA

Adverse events under product code DSA

product code DSA
Death
2
Total
2

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code DSA

1–100 of 105

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