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

Stocking, Elastic

21 CFR 890.3475 / Physical Medicine
FDA source (opens on fda.gov)

ILG is the FDA product code for Stocking, Elastic, a class I device type, regulated under 21 CFR 890.3475. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
ILG
Device name
Stocking, Elastic
Regulation
21 CFR 890.3475
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
8
Ingested recalls
3

Clearances, product code ILG

By decision year
8 clearances under product code ILG with a decision year between 1976 and 1983, 1976 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code ILG by decision year
YearClearances
19762
19772
19782
19832

Applicants with the most clearances

Product code ILG
Applicants holding the most 510(k) clearances under product code ILG
ApplicantClearances
Abco Dealers, Inc.1
Alba-Waldensian, Inc.1
Chase Mfg. Co.1
Convertors1
Fred Sammons, Inc.1
Northern Medical Surgical, Inc.1
Parke-Davis Co.1
Richard'S Medical Equip., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 92 companies shown, in name order