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

Battery, Replacement, Rechargeable

21 CFR 878.4820 / General, Plastic Surgery
FDA source (opens on fda.gov)

MOQ is the FDA product code for Battery, Replacement, Rechargeable, a class I device type, regulated under 21 CFR 878.4820. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
MOQ
Device name
Battery, Replacement, Rechargeable
Regulation
21 CFR 878.4820
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
3
Ingested recalls
6

Clearances, product code MOQ

By decision year
3 clearances under product code MOQ with a decision year between 1998 and 2008, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MOQ by decision year
YearClearances
19981
20011
20081

Applicants with the most clearances

Product code MOQ
Applicants holding the most 510(k) clearances under product code MOQ
ApplicantClearances
Alexander Mfg. Co.1
Nordix, Inc.1
Teleflex Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 45 companies shown, in name order