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

Rongeur, Cystoscopic, Hot

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

KDO is the FDA product code for Rongeur, Cystoscopic, Hot, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KDO
Device name
Rongeur, Cystoscopic, Hot
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
1
Ingested recalls
0

Clearances, product code KDO

By decision year
1 clearance under product code KDO with a decision year between 1993 and 1993, 1993 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KDO by decision year
YearClearances
19931

Applicants with the most clearances

Product code KDO
Applicants holding the most 510(k) clearances under product code KDO
ApplicantClearances
Westmark Hospital Supplies1

Companies listing this code with FDA

Companies whose registered establishments list this code

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