Cleared Traditional

CLAMP, TUBING, LINE (K844121) - FDA 510(k) Clearance

Class I Gastroenterology & Urology device.

K844121 · Dyn-A-Med Products · Gastroenterology & Urology device
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Dec 1984
Decision
55d
Days
Class 1
Risk

K844121 is an FDA 510(k) clearance for the CLAMP, TUBING, LINE. Classified as Clamp, Line (product code FKK), Class I - General Controls.

Submitted by Dyn-A-Med Products (Barrington, US). The FDA issued a Cleared decision on December 17, 1984 after a review of 55 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4730 - the FDA gastroenterology and urology 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.

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Submission Details

510(k) Number K844121 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 1984
Decision Date December 17, 1984
Days to Decision 55 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 130d · This submission: 55d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FKK Clamp, Line
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.4730
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.