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

System, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use)

21 CFR 884.2982 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KYA is the FDA product code for System, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use), a class I device type, regulated under 21 CFR 884.2982. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KYA
Device name
System, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use)
Regulation
21 CFR 884.2982
Device class
Class I
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code KYA

By decision year
5 clearances under product code KYA with a decision year between 1982 and 1990, 1982 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KYA by decision year
YearClearances
19823
19841
19901

Applicants with the most clearances

Product code KYA
Applicants holding the most 510(k) clearances under product code KYA
ApplicantClearances
American Thermometer Company, Inc.2
Bcsi Laboratories, Inc.1
Dr. John D. Reid B.A., D.C.1
Promedex, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code