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

Chair And Table, Medical

21 CFR 880.6140 / General Hospital
FDA source (opens on fda.gov)

KMN is the FDA product code for Chair And Table, Medical, a class I device type, regulated under 21 CFR 880.6140. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
KMN
Device name
Chair And Table, Medical
Regulation
21 CFR 880.6140
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
3
Ingested recalls
3

Clearances, product code KMN

By decision year
3 clearances under product code KMN with a decision year between 1976 and 1989, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KMN by decision year
YearClearances
19761
19801
19891

Applicants with the most clearances

Product code KMN
Applicants holding the most 510(k) clearances under product code KMN
ApplicantClearances
Fred Sammons, Inc.1
M.D. Intl., Inc.1
Volunteer Blind Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 180 companies shown, in name order