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

Massager, Therapeutic, Manual

21 CFR 890.5660 / Physical Medicine
FDA source (opens on fda.gov)

LYG is the FDA product code for Massager, Therapeutic, Manual, a class I device type, regulated under 21 CFR 890.5660. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LYG
Device name
Massager, Therapeutic, Manual
Regulation
21 CFR 890.5660
Device class
Class I
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
13
Ingested recalls
0

Clearances, product code LYG

By decision year
13 clearances under product code LYG with a decision year between 1988 and 1996, 1988 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LYG by decision year
YearClearances
19883
19901
19912
19921
19931
19942
19951
19962

Applicants with the most clearances

Product code LYG
Applicants holding the most 510(k) clearances under product code LYG
ApplicantClearances
Ferguson Medical2
Alain Machtelinckx1
Arocep Enterprises, Ltd.1
Dambrecine, Inc.1
Eight Corners, Inc.1
Focus International, Inc.1
Four Directions1
Innova Corp.1
Mckenna & Cuneo1
Medical Flotation Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 178 companies shown, in name order