510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831079Substantially Equivalent

Liquipette

The Kendall Company Div. of Tyco Healthcare Group, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831079 is the FDA 510(k) clearance record for LIQUIPETTE, a class I device, cleared for The Kendall Company Div. of Tyco Healthcare Group on under FDA product code GJG (Pipette, Quantitative, Hematology). FDA records list 4 510(k) clearances for The Kendall Company Div. of Tyco Healthcare Group, from to . As of , FDA records show no recalls naming K831079.

Clearance record

Decision date
Received
(24 days to decision)
Product code
GJG Pipette, Quantitative, Hematology
Regulation
21 CFR 864.6160
Device class
Class I
Review panel
Hematology
Applicant
The Kendall Company Div. of Tyco Healthcare Group 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GJG

Trailing 12 months

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

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