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
KGDClass II

Scissors For Cystoscope

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

KGD is the FDA product code for Scissors For Cystoscope, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KGD
Device name
Scissors For Cystoscope
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
2
Ingested recalls
0

Clearances, product code KGD

By decision year
2 clearances under product code KGD with a decision year between 1989 and 1994, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KGD by decision year
YearClearances
19891
19941

Applicants with the most clearances

Product code KGD
Applicants holding the most 510(k) clearances under product code KGD
ApplicantClearances
Arent Fox1
Zinnanti Surgical Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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