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

Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered

21 CFR 886.4100 / Ophthalmic
FDA source (opens on fda.gov)

NCR is the FDA product code for Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered, a class II device type, regulated under 21 CFR 886.4100. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
NCR
Device name
Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered
Regulation
21 CFR 886.4100
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
1

Clearances, product code NCR

By decision year
3 clearances under product code NCR with a decision year between 2000 and 2005, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NCR by decision year
YearClearances
20001
20041
20051

Applicants with the most clearances

Product code NCR
Applicants holding the most 510(k) clearances under product code NCR
ApplicantClearances
Medisurg, Ltd.3

Companies listing this code with FDA

Companies whose registered establishments list this code