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

Anti-Ribosomal P Antibodies

21 CFR 866.5100 / Immunology
FDA source (opens on fda.gov)

MQA is the FDA product code for Anti-Ribosomal P Antibodies, a class II device type, regulated under 21 CFR 866.5100. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MQA
Device name
Anti-Ribosomal P Antibodies
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code MQA

By decision year
4 clearances under product code MQA with a decision year between 1996 and 2021, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MQA by decision year
YearClearances
19961
19981
20031
20211

Applicants with the most clearances

Product code MQA
Applicants holding the most 510(k) clearances under product code MQA
ApplicantClearances
Hogan & Hartson1
Inova Diagnostics, Inc.1
Phadia AB1
Theratest Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code