510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930328Substantially Equivalent

Navigator & Traveler Evoked Postential Product

Bio-Logic Systems Corp., Mudelein IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930328 is the FDA 510(k) clearance record for NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT, a class II device, cleared for Bio-Logic Systems Corp. on under FDA product code IKN (Electromyograph, Diagnostic). FDA records list 57 510(k) clearances for Bio-Logic Systems Corp., from to . As of , FDA records show no recalls naming K930328.

Clearance record

Decision date
Received
(161 days to decision)
Product code
IKN Electromyograph, Diagnostic
Regulation
21 CFR 890.1375
Device class
Class II
Review panel
Physical Medicine
Applicant
Bio-Logic Systems Corp. One Bio-Logic Plz., Mudelein IL
510(k) summary
Statement
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