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
K884403Substantially Equivalent

Liquid Chromatography Columns Solid Phase Ex. Tube

Supelco, Inc., Bellefonte PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884403 is the FDA 510(k) clearance record for LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE, a class I device, cleared for Supelco, Inc. on under FDA product code DPM (Columns, Liquid Chromatography). FDA records list 24 510(k) clearances for Supelco, Inc., from to . As of , FDA records show no recalls naming K884403.

Clearance record

Decision date
Received
(64 days to decision)
Product code
DPM Columns, Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Supelco, Inc. Supelco Park, Bellefonte PA
Third party review
No

Clearances, product code DPM

Trailing 12 months

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

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