510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760389Substantially Equivalent

Cannula, IV

B. Braun Instruments, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760389 is the FDA 510(k) clearance record for CANNULA, IV, a class I device, cleared for B. Braun Instruments on under FDA product code FGY (Cannula, Injection). FDA records list 13 510(k) clearances for B. Braun Instruments. As of , FDA records show no recalls naming K760389.

Clearance record

Decision date
Received
(89 days to decision)
Product code
FGY Cannula, Injection
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
B. Braun Instruments 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FGY

Trailing 12 months

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

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