510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862148Substantially Equivalent

Olympus Au 5000 Flame Photometer Module

Olympus Corp., Lake Success NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862148 is the FDA 510(k) clearance record for OLYMPUS AU 5000 FLAME PHOTOMETER MODULE, a class I device, cleared for Olympus Corp. on under FDA product code JJO (Flame Emission Photometer For Clinical Use). FDA records list 149 510(k) clearances for Olympus Corp., from to . As of , FDA records show no recalls naming K862148.

Clearance record

Decision date
Received
(117 days to decision)
Product code
JJO Flame Emission Photometer For Clinical Use
Regulation
21 CFR 862.2540
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Olympus Corp. 4 Nevada Dr., Lake Success NY
Third party review
No

Clearances, product code JJO

Trailing 12 months

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

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