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

Source, Chemiluminescent Light

21 CFR 884.4530 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MPU is the FDA product code for Source, Chemiluminescent Light, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MPU
Device name
Source, Chemiluminescent Light
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
1

Clearances, product code MPU

By decision year
2 clearances under product code MPU with a decision year between 1997 and 2001, 1997 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MPU by decision year
YearClearances
19971
20011

Applicants with the most clearances

Product code MPU
Applicants holding the most 510(k) clearances under product code MPU
ApplicantClearances
Trylon Corp.2

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MPU.