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

Ophthalmoscopes, Replacement Batteries, Hand-Held

21 CFR 886.1570 / Ophthalmic
FDA source (opens on fda.gov)

MSG is the FDA product code for Ophthalmoscopes, Replacement Batteries, Hand-Held, a class II device type, regulated under 21 CFR 886.1570. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MSG
Device name
Ophthalmoscopes, Replacement Batteries, Hand-Held
Regulation
21 CFR 886.1570
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MSG

By decision year
2 clearances under product code MSG with a decision year between 1997 and 1997, 1997 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MSG by decision year
YearClearances
19972

Applicants with the most clearances

Product code MSG
Applicants holding the most 510(k) clearances under product code MSG
ApplicantClearances
Alexander Mfg. Co.2

Companies listing this code with FDA

Companies whose registered establishments list this code