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

System, Communication, Powered

21 CFR 890.3710 / Physical Medicine
FDA source (opens on fda.gov)

ILQ is the FDA product code for System, Communication, Powered, a class II device type, regulated under 21 CFR 890.3710. As of , FDA records hold 38 510(k) clearances under this code, the most recent dated , and 19 recalls.

Classification record

Product code
ILQ
Device name
System, Communication, Powered
Regulation
21 CFR 890.3710
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
38
Ingested recalls
19

Clearances, product code ILQ

By decision year
38 clearances under product code ILQ with a decision year between 1977 and 2017, 1990 the highest year at 7.
Show the numbers
510(k) clearances under FDA product code ILQ by decision year
YearClearances
19774
19812
19821
19831
19842
19862
19891
19907
19914
19922
19936
19945
20171

Applicants with the most clearances

Product code ILQ
Applicants holding the most 510(k) clearances under product code ILQ
ApplicantClearances
Prentke Romich Co.4
Zygo Industries, Inc.4
Med Labs, Inc.3
Possum, Inc.3
Baylor Biomedical Services2
Companion Products Intl.2
Almicro Electronics, Inc.1
C.R. Bard Inc1
Carepartners, Inc.1
Convaid, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 45 companies shown, in name order