Cleared Traditional

K770169 - BEESON AUTOMADDAK FEEDER

K770169 is the FDA 510(k) clearance for BEESON AUTOMADDAK FEEDER by Techhnilab Instruments, Inc.. It is a Class 1 Physical Medicine device (product code ILC) cleared through the Traditional 510(k) pathway after a 3-day FDA review.

K770169 · Techhnilab Instruments, Inc. · Physical Medicine device
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Jan 1977
Decision
3d
Days
Class 1
Risk

K770169 is an FDA 510(k) clearance for the BEESON AUTOMADDAK FEEDER. Classified as Utensil, Eating (product code ILC), Class I - General Controls.

Submitted by Techhnilab Instruments, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 28, 1977 after a review of 3 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5050 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Techhnilab Instruments, Inc. devices

Submission Details

510(k) Number K770169 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1977
Decision Date January 28, 1977
Days to Decision 3 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 115d · This submission: 3d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code ILC Utensil, Eating
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5050
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - ILC Utensil, Eating

All 29
Devices cleared under the same product code (ILC) and FDA review panel - the closest regulatory comparables to K770169.
KNIFE, LARGE HANDLE
K781193 · Fred Sammons, Inc. · Jul 1978
UTENSILS, WEIGHTED
K781196 · Fred Sammons, Inc. · Jul 1978
QUADRIPLEGIC MEAT KNIFE
K771274 · Fred Sammons, Inc. · Jul 1977
ADULT SWIVEL FORK
K761104 · Fred Sammons, Inc. · Dec 1976
WEIGHTED SPORK
K761105 · Fred Sammons, Inc. · Dec 1976
WEIGHTED FORK
K761106 · Fred Sammons, Inc. · Dec 1976