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

Syringe, Ent

21 CFR 874.5220 / Ear, Nose, Throat
FDA source (opens on fda.gov)

KCP is the FDA product code for Syringe, Ent, a class I device type, regulated under 21 CFR 874.5220. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
KCP
Device name
Syringe, Ent
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
4
Ingested recalls
1

Clearances, product code KCP

By decision year
4 clearances under product code KCP with a decision year between 1978 and 1984, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KCP by decision year
YearClearances
19781
19811
19821
19841

Applicants with the most clearances

Product code KCP
Applicants holding the most 510(k) clearances under product code KCP
ApplicantClearances
Abco Dealers, Inc.1
American Hospital Supply1
Imm Enterprises, Ltd.1
R. Wolf Medical Instruments Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 141 companies shown, in name order