510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K913705Substantially Equivalent

Abbott Qluickstart Iron Test, Item #5A29

Em Diagnostic Systems, Inc., Gibbstown NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913705 is the FDA 510(k) clearance record for ABBOTT QLUICKSTART IRON TEST, ITEM #5A29, a class I device, cleared for Em Diagnostic Systems, Inc. on under FDA product code CFM (Bathophenanthroline, Colorimetry, Iron (Non-Heme)). FDA records list 288 510(k) clearances for Em Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K913705.

Clearance record

Decision date
Received
(51 days to decision)
Product code
CFM Bathophenanthroline, Colorimetry, Iron (Non-Heme)
Regulation
21 CFR 862.1410
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Em Diagnostic Systems, Inc. 480 Democrat Rd., Gibbstown NJ
510(k) summary
Statement
Third party review
No

Clearances, product code CFM

Trailing 12 months

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

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