510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770169Substantially Equivalent

Beeson Automaddak Feeder

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

K770169 is the FDA 510(k) clearance record for BEESON AUTOMADDAK FEEDER, a class I device, cleared for Techhnilab Instruments, Inc. on under FDA product code ILC (Utensil, Eating). FDA records list 6 510(k) clearances for Techhnilab Instruments, Inc., from to . As of , FDA records show no recalls naming K770169.

Clearance record

Decision date
Received
(3 days to decision)
Product code
ILC Utensil, Eating
Regulation
21 CFR 890.5050
Device class
Class I
Review panel
Physical Medicine
Applicant
Techhnilab Instruments, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ILC

Trailing 12 months

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

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