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

Scrapper, Skin Specimen

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

LXK is the FDA product code for Scrapper, Skin Specimen, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LXK
Device name
Scrapper, Skin Specimen
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
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
0

Clearances, product code LXK

By decision year
1 clearance under product code LXK with a decision year between 1988 and 1988, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LXK by decision year
YearClearances
19881

Applicants with the most clearances

Product code LXK
Applicants holding the most 510(k) clearances under product code LXK
ApplicantClearances
Ortho Pharmaceutical Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code