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

Absorber, Saliva, Paper

21 CFR 872.6050 / Dental
FDA source (opens on fda.gov)

KHR is the FDA product code for Absorber, Saliva, Paper, a class I device type, regulated under 21 CFR 872.6050. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KHR
Device name
Absorber, Saliva, Paper
Regulation
21 CFR 872.6050
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
10
Ingested recalls
0

Clearances, product code KHR

By decision year
10 clearances under product code KHR with a decision year between 1977 and 1998, 1989 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KHR by decision year
YearClearances
19771
19781
19851
19871
19893
19952
19981

Applicants with the most clearances

Product code KHR
Applicants holding the most 510(k) clearances under product code KHR
ApplicantClearances
3M Company1
Adri1
American Orthodontics1
Dispomed, Inc.1
E.H. Medical Co.1
Irt Management Corp.1
Microcopy, Div. Neo-Flo, Inc.1
Nice-Pak Products, LLC1
Physician Industries, Inc.1
Remington Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 148 companies shown, in name order