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

Label Or Tag, Sterile

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

LYV is the FDA product code for Label Or Tag, Sterile, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LYV
Device name
Label Or Tag, Sterile
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
2
Ingested recalls
0

Clearances, product code LYV

By decision year
2 clearances under product code LYV with a decision year between 1988 and 1988, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LYV by decision year
YearClearances
19882

Applicants with the most clearances

Product code LYV
Applicants holding the most 510(k) clearances under product code LYV
ApplicantClearances
Acacia Laboratories, Inc.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 60 companies shown, in name order