510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K894272Substantially Equivalent

Denley Welldill 3

Denley Instruments, Inc., Durham NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894272 is the FDA 510(k) clearance record for DENLEY WELLDILL 3, a class I device, cleared for Denley Instruments, Inc. on under FDA product code JQW (Station, Pipetting And Diluting, For Clinical Use). FDA records list 9 510(k) clearances for Denley Instruments, Inc., from to . As of , FDA records show no recalls naming K894272.

Clearance record

Decision date
Received
(60 days to decision)
Product code
JQW Station, Pipetting And Diluting, For Clinical Use
Regulation
21 CFR 862.2750
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Denley Instruments, Inc. 4905 Pine Cone Dr., Suite 3, Durham NC
Third party review
No

Clearances, product code JQW

Trailing 12 months

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

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