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

Strip, Temperature, Forehead, Liquid Crystal

21 CFR 880.2200 / General Hospital
FDA source (opens on fda.gov)

KPD is the FDA product code for Strip, Temperature, Forehead, Liquid Crystal, a class II device type, regulated under 21 CFR 880.2200. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KPD
Device name
Strip, Temperature, Forehead, Liquid Crystal
Regulation
21 CFR 880.2200
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
21
Ingested recalls
0

Clearances, product code KPD

By decision year
21 clearances under product code KPD with a decision year between 1976 and 1994, 1977 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KPD by decision year
YearClearances
19761
19773
19782
19791
19801
19811
19823
19833
19841
19851
19871
19891
19901
19941

Applicants with the most clearances

Product code KPD
Applicants holding the most 510(k) clearances under product code KPD
ApplicantClearances
Biosynergy, Inc.2
Respiratory Care, Inc.2
T. G. & E. Medical2
American Thermal Instruments, LLC1
American Thermometer Company, Inc.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Djinnii Industires, Inc.1
Inhal-O-Tech Medical Plastic1
Liquid Crystal Products, Inc.1
Liquid Crystal Sciences, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 40 companies shown, in name order