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

Syringe, Antistick

21 CFR 880.5860 / General Hospital
FDA source (opens on fda.gov)

MEG is the FDA product code for Syringe, Antistick, a class II device type, regulated under 21 CFR 880.5860. As of , FDA records hold 162 510(k) clearances under this code, the most recent dated , and 17 recalls.

Classification record

Product code
MEG
Device name
Syringe, Antistick
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
162
Ingested recalls
17

Clearances, product code MEG

By decision year
162 clearances under product code MEG with a decision year between 1994 and 2026, 2022 the highest year at 13.
Show the numbers
510(k) clearances under FDA product code MEG by decision year
YearClearances
19942
19956
19961
19972
19985
19992
20006
20019
20027
200311
200411
200512
200610
20078
20084
20092
20102
20115
20125
20131
20145
20157
20163
20173
20181
20194
20203
20215
202213
20235
20251
20261

Applicants with the most clearances

Product code MEG
Applicants holding the most 510(k) clearances under product code MEG
ApplicantClearances
Safety Syringes, Inc.7
Life-Shield Products, Inc.5
MK Meditech5
Biotop Technology Co., Ltd.4
Retractable Technologies, Inc.4
Shantou Wealy Medical Instrument Co., Ltd.4
Taiject Medical Device Co., Ltd.4
Formosa Medical Devices, Inc.3
Inviro Medical Devices, Inc.3
Abbott Medical3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 126 companies shown, in name order