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

Accessories To Examination Light

21 CFR 880.6320 / General Hospital
FDA source (opens on fda.gov)

PEQ is the FDA product code for Accessories To Examination Light, a class I device type, regulated under 21 CFR 880.6320. FDA's definition for this code reads: "Accessories that attach to the light and assist in magnifying, clarifying, enhancing the image being viewed". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
PEQ
Device name
Accessories To Examination Light
FDA definition
Accessories that attach to the light and assist in magnifying, clarifying, enhancing the image being viewed.
Regulation
21 CFR 880.6320
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code PEQ

By decision year
1 clearance under product code PEQ with a decision year between 2013 and 2013, 2013 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code PEQ by decision year
YearClearances
20131

Applicants with the most clearances

Product code PEQ
Applicants holding the most 510(k) clearances under product code PEQ
ApplicantClearances
Globalmedia Group, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code