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

Phlebograph, Impedance

21 CFR 870.2750 / Cardiovascular
FDA source (opens on fda.gov)

DQB is the FDA product code for Phlebograph, Impedance, a class II device type, regulated under 21 CFR 870.2750. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DQB
Device name
Phlebograph, Impedance
Regulation
21 CFR 870.2750
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
3
Ingested recalls
0

Clearances, product code DQB

By decision year
3 clearances under product code DQB with a decision year between 1977 and 1985, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DQB by decision year
YearClearances
19771
19831
19851

Applicants with the most clearances

Product code DQB
Applicants holding the most 510(k) clearances under product code DQB
ApplicantClearances
Dynatech Research & Development Co.1
Eko Scann AB1
Sonicaid, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DQB.