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

Device, Pressure Applying

21 CFR 890.5765 / Physical Medicine
FDA source (opens on fda.gov)

KNM is the FDA product code for Device, Pressure Applying, a class I device type, regulated under 21 CFR 890.5765. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KNM
Device name
Device, Pressure Applying
Regulation
21 CFR 890.5765
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code KNM

By decision year
2 clearances under product code KNM with a decision year between 1978 and 1981, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KNM by decision year
YearClearances
19781
19811

Applicants with the most clearances

Product code KNM
Applicants holding the most 510(k) clearances under product code KNM
ApplicantClearances
Autonomic Equipment Supply Co2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 67 companies shown, in name order