510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K922858Unknown

Multidraw System

Cambridge Multi-Draw, Inc., Cambridge MA / Traditional, Unknown
FDA source (opens on fda.gov)

K922858 is the FDA 510(k) clearance record for MULTIDRAW SYSTEM, a class II device, cleared for Cambridge Multi-Draw, Inc. on under FDA product code GIM (Tubes, Vacuum Sample, With Anticoagulant). FDA records list one 510(k) clearance for Cambridge Multi-Draw, Inc. As of , FDA records show no recalls naming K922858.

Clearance record

Decision date
Received
(154 days to decision)
Product code
GIM Tubes, Vacuum Sample, With Anticoagulant
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Cambridge Multi-Draw, Inc. 56 Creighton St., Cambridge MA
510(k) summary
Statement
Third party review
No

Clearances, product code GIM

Trailing 12 months

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

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