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

System, Communication, Non-Powered

21 CFR 890.3700 / Physical Medicine
FDA source (opens on fda.gov)

ILP is the FDA product code for System, Communication, Non-Powered, a class I device type, regulated under 21 CFR 890.3700. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
ILP
Device name
System, Communication, Non-Powered
Regulation
21 CFR 890.3700
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
21
Ingested recalls
0

Clearances, product code ILP

By decision year
21 clearances under product code ILP with a decision year between 1976 and 1985, 1982 the highest year at 12.
Show the numbers
510(k) clearances under FDA product code ILP by decision year
YearClearances
19761
19771
19781
19813
198212
19831
19841
19851

Applicants with the most clearances

Product code ILP
Applicants holding the most 510(k) clearances under product code ILP
ApplicantClearances
Fred Sammons, Inc.18
Joseph A. Resnick1
Mina Manufacturers, Inc.1
Possum, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code