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KNM

2 FDA 510(k) clearances · Product code

FDA profile

Official device name
Device, Pressure Applying
Device class
Class I (low risk)
Regulation
21 CFR 890.5765
Medical specialty
Physical Medicine
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RecordFirmDate
AUTONORM & NERV-A-NORM (K811956)Autonomic Equipment Supply Co,1981-07-31
AUTONOM (K780312)Autonomic Equipment Supply Co,1978-04-05

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Every clearance here is in the API, with alerts when new ones post.