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

Monitor, Pressure, Intracompartmental

Unknown
FDA source (opens on fda.gov)

LXC is the FDA product code for Monitor, Pressure, Intracompartmental. As of , FDA records hold 15 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
LXC
Device name
Monitor, Pressure, Intracompartmental
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
15
Ingested recalls
2

Clearances, product code LXC

By decision year
15 clearances under product code LXC with a decision year between 1985 and 2026, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LXC by decision year
YearClearances
19851
19882
20031
20041
20061
20091
20141
20202
20211
20221
20231
20251
20261

Applicants with the most clearances

Product code LXC
Applicants holding the most 510(k) clearances under product code LXC
ApplicantClearances
MY01, Inc.6
Twin Star Medical, Inc.4
Ace Medical1
Buckman Co., Inc.1
Compremium AG1
Stryker Corp.1
Synthes (USA) Products LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code