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

Diazo, Ast/Sgot

21 CFR 862.1100 / Clinical Chemistry
FDA source (opens on fda.gov)

CIQ is the FDA product code for Diazo, Ast/Sgot, a class II device type, regulated under 21 CFR 862.1100. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
CIQ
Device name
Diazo, Ast/Sgot
Regulation
21 CFR 862.1100
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
1

Clearances, product code CIQ

By decision year
7 clearances under product code CIQ with a decision year between 1982 and 1988, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CIQ by decision year
YearClearances
19822
19842
19862
19881

Applicants with the most clearances

Product code CIQ
Applicants holding the most 510(k) clearances under product code CIQ
ApplicantClearances
Anco Medical Reagents & Assoc.1
Livonia Diagnostics, Inc.1
Medical Specialties Inc.1
Omega Medical Electronics1
Sterling Diagnostics, Inc.1
Tech-Co, Inc.1
Technostics Intl.1

Companies listing this code with FDA

Companies whose registered establishments list this code