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

Reminder, Medication

21 CFR 890.5050 / Physical Medicine
FDA source (opens on fda.gov)

NXQ is the FDA product code for Reminder, Medication, a class I device type, regulated under 21 CFR 890.5050. FDA's definition for this code reads: "A medication reminder is a device intended for medical purposes to provide alerts to patients or healthcare providers for pre-determined medication dosing schedules. The device may incorporate wireless communication". As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
NXQ
Device name
Reminder, Medication
FDA definition
A medication reminder is a device intended for medical purposes to provide alerts to patients or healthcare providers for pre-determined medication dosing schedules. The device may incorporate wireless communication.
Regulation
21 CFR 890.5050
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
1

Clearances, product code NXQ

By decision year
2 clearances under product code NXQ with a decision year between 2006 and 2011, 2006 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NXQ by decision year
YearClearances
20061
20111

Applicants with the most clearances

Product code NXQ
Applicants holding the most 510(k) clearances under product code NXQ
ApplicantClearances
Senticare, Inc.1
Vocel1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 60 companies shown, in name order