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

Detector, Ultraviolet

21 CFR 872.6350 / Dental
FDA source (opens on fda.gov)

EAQ is the FDA product code for Detector, Ultraviolet, a class II device type, regulated under 21 CFR 872.6350. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EAQ
Device name
Detector, Ultraviolet
Regulation
21 CFR 872.6350
Device class
Class II
Review panel
Dental
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code EAQ

By decision year
2 clearances under product code EAQ with a decision year between 1977 and 1994, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EAQ by decision year
YearClearances
19771
19941

Applicants with the most clearances

Product code EAQ
Applicants holding the most 510(k) clearances under product code EAQ
ApplicantClearances
Parker Laboratories, Inc.1
Sunsor, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code