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

Liquid Chemical Processing System

21 CFR 880.6887 / General Hospital
FDA source (opens on fda.gov)

OVY is the FDA product code for Liquid Chemical Processing System, a class II device type, regulated under 21 CFR 880.6887. FDA's definition for this code reads: "The liquid chemical processing system is intended as a standard method for routine monitoring". As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
OVY
Device name
Liquid Chemical Processing System
FDA definition
The liquid chemical processing system is intended as a standard method for routine monitoring.
Regulation
21 CFR 880.6887
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code OVY

By decision year
4 clearances under product code OVY with a decision year between 2012 and 2023, 2023 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code OVY by decision year
YearClearances
20121
20181
20232

Applicants with the most clearances

Product code OVY
Applicants holding the most 510(k) clearances under product code OVY
ApplicantClearances
STERIS Corporation4

Companies listing this code with FDA

Companies whose registered establishments list this code