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

Applicator, Absorbent Tipped, Sterile

21 CFR 880.6025 / General Hospital
FDA source (opens on fda.gov)

KXG is the FDA product code for Applicator, Absorbent Tipped, Sterile, a class I device type, regulated under 21 CFR 880.6025. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 10 recalls.

Classification record

Product code
KXG
Device name
Applicator, Absorbent Tipped, Sterile
Regulation
21 CFR 880.6025
Device class
Class I
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
1
Ingested recalls
10

Clearances, product code KXG

By decision year
1 clearance under product code KXG with a decision year between 1980 and 1980, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KXG by decision year
YearClearances
19801

Applicants with the most clearances

Product code KXG
Applicants holding the most 510(k) clearances under product code KXG
ApplicantClearances
Pollak (Intl.).ltd1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 267 companies shown, in name order