Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K800690Substantially Equivalent

Reagent for Determ. Inorganic/phosphorus

Diagnostic Solutions, Inc., Mchenry IL / Traditional, Substantially Equivalent

K800690 is the FDA 510(k) clearance record for REAGENT FOR DETERM. INORGANIC/PHOSPHORUS, a class I device, cleared for Diagnostic Solutions, Inc. on under FDA product code CEO (Phosphomolybdate (Colorimetric), Inorganic Phosphorus). FDA records list 26 510(k) clearances for Diagnostic Solutions, Inc., from to . As of , FDA records show no recalls naming K800690.

Clearance record

Decision date
Received
(63 days to decision)
Product code
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Regulation
21 CFR 862.1580
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Diagnostic Solutions, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CEO

Trailing 12 months

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

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