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
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K022895Substantially Equivalent

Elcam Stopcocks and Manifolds

Medical Device Consultants, Inc., North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K022895 is the FDA 510(k) clearance record for ELCAM STOPCOCKS AND MANIFOLDS, a class II device, cleared for Medical Device Consultants, Inc. on under FDA product code FMG (Stopcock, I.V. Set). FDA records list 14 510(k) clearances for Medical Device Consultants, Inc., from to . As of , FDA records show 14 recalls naming K022895.

Clearance record

Decision date
Received
(45 days to decision)
Product code
FMG Stopcock, I.V. Set
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Medical Device Consultants, Inc. 49 Plain St., North Attleboro MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FMG

Trailing 12 months

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

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