510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DYCClass II

Vectorcardiograph

21 CFR 870.2400 / Cardiovascular
FDA source (opens on fda.gov)

DYC is the FDA product code for Vectorcardiograph, a class II device type, regulated under 21 CFR 870.2400. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DYC
Device name
Vectorcardiograph
Regulation
21 CFR 870.2400
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code DYC

By decision year
4 clearances under product code DYC with a decision year between 1981 and 2003, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DYC by decision year
YearClearances
19811
19831
19901
20031

Applicants with the most clearances

Product code DYC
Applicants holding the most 510(k) clearances under product code DYC
ApplicantClearances
Elmed, Inc.1
Medical Graphics Corp.1
Odam1
Ortivus AB1

Companies listing this code with FDA

Companies whose registered establishments list this code