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

Magnet, Ac-Powered

21 CFR 886.4440 / Ophthalmic
FDA source (opens on fda.gov)

HPO is the FDA product code for Magnet, Ac-Powered, a class II device type, regulated under 21 CFR 886.4440. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HPO
Device name
Magnet, Ac-Powered
Regulation
21 CFR 886.4440
Device class
Class II
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
3
Ingested recalls
0

Clearances, product code HPO

By decision year
3 clearances under product code HPO with a decision year between 1983 and 1986, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HPO by decision year
YearClearances
19832
19861

Applicants with the most clearances

Product code HPO
Applicants holding the most 510(k) clearances under product code HPO
ApplicantClearances
JEDMED Instrument Company1
Mira, Inc.1
Scientific Manufacturer1

Companies listing this code with FDA

Companies whose registered establishments list this code