510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883781Substantially Equivalent

Nicolet Neuroport/ace System

Nicolet Instrument Corp., Madison WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883781 is the FDA 510(k) clearance record for NICOLET NEUROPORT/ACE SYSTEM, a class II device, cleared for Nicolet Instrument Corp. on under FDA product code IKN (Electromyograph, Diagnostic). FDA records list 13 510(k) clearances for Nicolet Instrument Corp., from to . As of , FDA records show no recalls naming K883781.

Clearance record

Decision date
Received
(272 days to decision)
Product code
IKN Electromyograph, Diagnostic
Regulation
21 CFR 890.1375
Device class
Class II
Review panel
Physical Medicine
Applicant
Nicolet Instrument Corp. 5225 Verona Rd., Madison WI
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