510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FFZClass II

Cord, Electric, For Endoscope

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FFZ is the FDA product code for Cord, Electric, For Endoscope, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
FFZ
Device name
Cord, Electric, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
1

Clearances, product code FFZ

By decision year
3 clearances under product code FFZ with a decision year between 1979 and 2011, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FFZ by decision year
YearClearances
19791
19821
20111

Applicants with the most clearances

Product code FFZ
Applicants holding the most 510(k) clearances under product code FFZ
ApplicantClearances
Concept, Inc.1
Kelleher Corp.1
Diversatek Healthcare Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code FFZ.