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

Analyzer, Nitric Oxide

21 CFR 868.2380 / Anesthesiology
FDA source (opens on fda.gov)

MRP is the FDA product code for Analyzer, Nitric Oxide, a class II device type, regulated under 21 CFR 868.2380. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MRP
Device name
Analyzer, Nitric Oxide
Regulation
21 CFR 868.2380
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MRP

By decision year
1 clearance under product code MRP with a decision year between 2003 and 2003, 2003 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MRP by decision year
YearClearances
20031

Applicants with the most clearances

Product code MRP
Applicants holding the most 510(k) clearances under product code MRP
ApplicantClearances
Pulmonox Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code