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

Burr, Corneal, Battery-Powered

21 CFR 886.4070 / Ophthalmic
FDA source (opens on fda.gov)

HOG is the FDA product code for Burr, Corneal, Battery-Powered, a class I device type, regulated under 21 CFR 886.4070. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOG
Device name
Burr, Corneal, Battery-Powered
Regulation
21 CFR 886.4070
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code HOG

By decision year
5 clearances under product code HOG with a decision year between 1984 and 1997, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HOG by decision year
YearClearances
19841
19891
19951
19961
19971

Applicants with the most clearances

Product code HOG
Applicants holding the most 510(k) clearances under product code HOG
ApplicantClearances
Apyx Medical Corporation1
Alcon Laboratories1
Gy-Ro Industry, Inc.1
JEDMED Instrument Company1
S. Percy Amoils1

Companies listing this code with FDA

Companies whose registered establishments list this code