Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K801833Substantially Equivalent

Gas-Chromatographic Packing

Supelco, Inc., Walker MI / Traditional, Substantially Equivalent

K801833 is the FDA 510(k) clearance record for GAS-CHROMATOGRAPHIC PACKING, a class I device, cleared for Supelco, Inc. on under FDA product code DJA (Column Supports, Glc). FDA records list 24 510(k) clearances for Supelco, Inc., from to . As of , FDA records show no recalls naming K801833.

Clearance record

Decision date
Received
(26 days to decision)
Product code
DJA Column Supports, Glc
Regulation
21 CFR 862.2250
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Supelco, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DJA

Trailing 12 months

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

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