510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863109Substantially Equivalent

Ferrofast

J. D. Assoc., Montclair NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863109 is the FDA 510(k) clearance record for FERROFAST, a class I device, cleared for J. D. Assoc. on under FDA product code JIY (Photometric Method, Iron (Non-Heme)). FDA records list 34 510(k) clearances for J. D. Assoc., from to . As of , FDA records show no recalls naming K863109.

Clearance record

Decision date
Received
(103 days to decision)
Product code
JIY Photometric Method, Iron (Non-Heme)
Regulation
21 CFR 862.1410
Device class
Class I
Review panel
Clinical Chemistry
Applicant
J. D. Assoc. 163 Montclair Ave., Montclair NJ
Third party review
No

Clearances, product code JIY

Trailing 12 months

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

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