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

Scissors, General, Surgical

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

LRW is the FDA product code for Scissors, General, Surgical, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 18 510(k) clearances under this code, the most recent dated , and 20 recalls.

Classification record

Product code
LRW
Device name
Scissors, General, 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
18
Ingested recalls
20

Clearances, product code LRW

By decision year
18 clearances under product code LRW with a decision year between 1985 and 1991, 1989 the highest year at 8.
Show the numbers
510(k) clearances under FDA product code LRW by decision year
YearClearances
19852
19872
19882
19898
19903
19911

Applicants with the most clearances

Product code LRW
Applicants holding the most 510(k) clearances under product code LRW
ApplicantClearances
Zinnanti Surgical Instruments, Inc.4
Artiberia2
Kinetic Medical Products2
Micrins, Ltd.2
Solos Endoscopy, Inc.2
Arthropedics, Inc.1
Dhason Brothers, Inc.1
Magnatrade Corp.1
Northgate Technologies Inc.1
Orion Life Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 502 companies shown, in name order