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

Processor, Radiographic-Film, Automatic, Dental

21 CFR 892.1900 / Radiology
FDA source (opens on fda.gov)

EGY is the FDA product code for Processor, Radiographic-Film, Automatic, Dental, a class II device type, regulated under 21 CFR 892.1900. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EGY
Device name
Processor, Radiographic-Film, Automatic, Dental
Regulation
21 CFR 892.1900
Device class
Class II
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
9
Ingested recalls
0

Clearances, product code EGY

By decision year
9 clearances under product code EGY with a decision year between 1977 and 1999, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EGY by decision year
YearClearances
19772
19811
19871
19901
19951
19962
19991

Applicants with the most clearances

Product code EGY
Applicants holding the most 510(k) clearances under product code EGY
ApplicantClearances
Ada Products Company, LLC1
Allied Photo Products Co., Inc.1
Denoptix, Inc.1
Dent-X Co.1
Dental X-Ray Support Systems, Inc.1
Gendex Corp.1
General Electric Co.1
Kaycor Intl., Ltd.1
Smith Companies Dental Products1

Companies listing this code with FDA

Companies whose registered establishments list this code