510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K874310Substantially Equivalent

Wire Dressing

Slocum and Neal, Inc., Columbia MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874310 is the FDA 510(k) clearance record for WIRE DRESSING, a class II device, cleared for Slocum and Neal, Inc. on under FDA product code LDF (Electrode, Pacemaker, Temporary). FDA records list one 510(k) clearance for Slocum and Neal, Inc. As of , FDA records show no recalls naming K874310.

Clearance record

Decision date
Received
(64 days to decision)
Product code
LDF Electrode, Pacemaker, Temporary
Regulation
21 CFR 870.3680
Device class
Class II
Review panel
Cardiovascular
Applicant
Slocum and Neal, Inc. 1804 Heirford, Columbia MO
Third party review
No

Clearances, product code LDF

Trailing 12 months
1 clearance under product code LDF in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LDF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260