510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802395Substantially Equivalent

Special Procedure Aqarose Film

Electrophoresis Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802395 is the FDA 510(k) clearance record for SPECIAL PROCEDURE AQAROSE FILM, a class I device, cleared for Electrophoresis Corp. on under FDA product code JJN (Apparatus, Electrophoresis, For Clinical Use). FDA records list 4 510(k) clearances for Electrophoresis Corp., from to . As of , FDA records show no recalls naming K802395.

Clearance record

Decision date
Received
(55 days to decision)
Product code
JJN Apparatus, Electrophoresis, For Clinical Use
Regulation
21 CFR 862.2485
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Electrophoresis Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JJN

Trailing 12 months

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

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