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

Tray, Surgical

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

LRP is the FDA product code for Tray, Surgical, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 22 510(k) clearances under this code, the most recent dated , and 108 recalls.

Classification record

Product code
LRP
Device name
Tray, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
22
Ingested recalls
109

Clearances, product code LRP

By decision year
22 clearances under product code LRP with a decision year between 1976 and 1996, 1988 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code LRP by decision year
YearClearances
19761
19861
19873
19884
19891
19901
19914
19931
19944
19951
19961

Applicants with the most clearances

Product code LRP
Applicants holding the most 510(k) clearances under product code LRP
ApplicantClearances
Apk Technology Co., Ltd2
Cush Medical Products2
Advantage Medical Systems, Inc.1
Angiosystems, Inc.1
Associated Medical1
CooperVision, Inc.1
Cushindu1
East Texas Lighthouse for the Blind1
Grand Medical Products1
J.J. Skinner, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 266 companies shown, in name order