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

Actuator, Syringe, Injector Type

21 CFR 870.1670 / Cardiovascular
FDA source (opens on fda.gov)

DQF is the FDA product code for Actuator, Syringe, Injector Type, a class II device type, regulated under 21 CFR 870.1670. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DQF
Device name
Actuator, Syringe, Injector Type
Regulation
21 CFR 870.1670
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 DQF

By decision year
3 clearances under product code DQF with a decision year between 1988 and 1992, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DQF by decision year
YearClearances
19882
19921

Applicants with the most clearances

Product code DQF
Applicants holding the most 510(k) clearances under product code DQF
ApplicantClearances
Alcon Laboratories1
Bioteque America Inc1
Spectramed, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code