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

Applicator, Ent Drug

21 CFR 874.5220 / Ear, Nose, Throat
FDA source (opens on fda.gov)

LRD is the FDA product code for Applicator, Ent Drug, a class I device type, regulated under 21 CFR 874.5220. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LRD
Device name
Applicator, Ent Drug
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
6
Ingested recalls
1

Clearances, product code LRD

By decision year
6 clearances under product code LRD with a decision year between 1992 and 1999, 1994 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LRD by decision year
YearClearances
19921
19931
19943
19991

Applicants with the most clearances

Product code LRD
Applicants holding the most 510(k) clearances under product code LRD
ApplicantClearances
Amsco Sterile Recoveries, Inc.1
Customed, Inc1
Denver Splint Co.1
Envis, Inc.1
Hospitak, Inc.1
The Merlin Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code