510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811956Substantially Equivalent

Autonorm & Nerv-a-Norm

Autonomic Equipment Supply Co, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811956 is the FDA 510(k) clearance record for AUTONORM & NERV-A-NORM, a class I device, cleared for Autonomic Equipment Supply Co, on under FDA product code KNM (Device, Pressure Applying). FDA records list 2 510(k) clearances for Autonomic Equipment Supply Co,, from to . As of , FDA records show no recalls naming K811956.

Clearance record

Decision date
Received
(22 days to decision)
Product code
KNM Device, Pressure Applying
Regulation
21 CFR 890.5765
Device class
Class I
Review panel
Physical Medicine
Applicant
Autonomic Equipment Supply Co, 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KNM

Trailing 12 months

FDA records hold no clearances under product code KNM in the trailing twelve months.

FDA records show no clearances under product code KNM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260