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

Pump, Infusion, Ophthalmic

21 CFR 880.5725 / General Hospital
FDA source (opens on fda.gov)

MRH is the FDA product code for Pump, Infusion, Ophthalmic, a class II device type, regulated under 21 CFR 880.5725. As of , FDA records hold 20 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MRH
Device name
Pump, Infusion, Ophthalmic
Regulation
21 CFR 880.5725
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
No
Ingested clearances
20
Ingested recalls
0

Clearances, product code MRH

By decision year
20 clearances under product code MRH with a decision year between 1996 and 2026, 1997 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MRH by decision year
YearClearances
19961
19972
19982
20002
20051
20131
20141
20172
20201
20212
20222
20231
20251
20261

Applicants with the most clearances

Product code MRH
Applicants holding the most 510(k) clearances under product code MRH
ApplicantClearances
Sight Sciences, Inc.8
New World Medical, Inc.2
Bausch & Lomb Incorporated1
Escalon Trek Medical1
Glaukos Corporation1
Iscience Surgical Corporation1
Medical Instrument Development Laboratories, Inc.1
Microsurgical Technologies, Inc.1
Peregrine Surgical, LLC.1
Retinalabs.Com1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order