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

Meter, Conductivity, Non-Remote

21 CFR 876.5820 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FIZ is the FDA product code for Meter, Conductivity, Non-Remote, a class II device type, regulated under 21 CFR 876.5820. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FIZ
Device name
Meter, Conductivity, Non-Remote
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
13
Ingested recalls
0

Clearances, product code FIZ

By decision year
13 clearances under product code FIZ with a decision year between 1978 and 2020, 2002 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FIZ by decision year
YearClearances
19781
19851
19871
19881
19931
19961
19981
19991
20022
20051
20151
20201

Applicants with the most clearances

Product code FIZ
Applicants holding the most 510(k) clearances under product code FIZ
ApplicantClearances
Mesa Laboratories Inc3
Automata Instrumentation, Inc.2
Automata Medical Instrumentation, Inc.2
Automata, Inc.2
Ibp Instruments GmbH2
Colorado Medical, Inc.1
Western Laboratories Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code