510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760815Substantially Equivalent

Fitting/dialyzer

Cobe Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760815 is the FDA 510(k) clearance record for FITTING/DIALYZER, a class II device, cleared for Cobe Laboratories, Inc. on under FDA product code FTG (Illuminator, Remote). FDA records list 77 510(k) clearances for Cobe Laboratories, Inc., from to . As of , FDA records show no recalls naming K760815.

Clearance record

Decision date
Received
(38 days to decision)
Product code
FTG Illuminator, Remote
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cobe Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FTG

Trailing 12 months

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

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