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

Slide Stainer, Immersion Type

21 CFR 864.3800 / Pathology
FDA source (opens on fda.gov)

KIO is the FDA product code for Slide Stainer, Immersion Type, a class I device type, regulated under 21 CFR 864.3800. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KIO
Device name
Slide Stainer, Immersion Type
Regulation
21 CFR 864.3800
Device class
Class I
Review panel
Pathology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code KIO

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

Applicants with the most clearances

Product code KIO
Applicants holding the most 510(k) clearances under product code KIO
ApplicantClearances
Shandon, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code