510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901732Substantially Equivalent

EMG Accessory for Posturography

Neurocom International, Inc., Clackamas OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901732 is the FDA 510(k) clearance record for EMG ACCESSORY FOR POSTUROGRAPHY, a class II device, cleared for Neurocom International, Inc. on under FDA product code IKN (Electromyograph, Diagnostic). FDA records list 5 510(k) clearances for Neurocom International, Inc., from to . As of , FDA records show no recalls naming K901732.

Clearance record

Decision date
Received
(511 days to decision)
Product code
IKN Electromyograph, Diagnostic
Regulation
21 CFR 890.1375
Device class
Class II
Review panel
Physical Medicine
Applicant
Neurocom International, Inc. 9570 SE Lawnfield Rd., Clackamas OR
Third party review
No

Clearances, product code IKN

Trailing 12 months

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

FDA records show no clearances under product code IKN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IKN, 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