510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K010217Substantially Equivalent

4 Port, 4 Way Stopcock

George Loo, MD, Beverly Hills CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010217 is the FDA 510(k) clearance record for 4 PORT, 4 WAY STOPCOCK, a class II device, cleared for George Loo, MD on under FDA product code FMG (Stopcock, I.V. Set). FDA records list one 510(k) clearance for George Loo, MD. As of , FDA records show no recalls naming K010217.

Clearance record

Decision date
Received
(53 days to decision)
Product code
FMG Stopcock, I.V. Set
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
George Loo, MD 9814 Curwood Pl., Beverly Hills CA
510(k) summary
Statement
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