Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K072536Substantially Equivalent

Esa Biosciences Inc. Vitamin D Hplc Test

Magellan Diagnostics, Inc., Chelmsford MA / Traditional, Substantially Equivalent

K072536 is the FDA 510(k) clearance record for ESA BIOSCIENCES INC. VITAMIN D HPLC TEST, a class II device, cleared for Esa Biosciences, Inc. on under FDA product code MRG (System, Test, Vitamin D). FDA records list 4 510(k) clearances for Magellan Diagnostics, Inc., from to . As of , FDA records show no recalls naming K072536.

Clearance record

Decision date
Received
(243 days to decision)
Product code
MRG System, Test, Vitamin D
Regulation
21 CFR 862.1825
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Esa Biosciences, Inc. 22 Alpha Rd., Chelmsford MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRG

Trailing 12 months

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

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