Cleared Traditional

VENA * BRIDGE (K840403) - FDA 510(k) Clearance

K840403 · Neward Enterprises, Inc. · Physical Medicine device
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Mar 1984
Decision
41d
Days
-
Risk

K840403 is an FDA 510(k) clearance for the VENA * BRIDGE.

Submitted by Neward Enterprises, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 12, 1984 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel. 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 Neward Enterprises, Inc. devices

Submission Details

510(k) Number K840403 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 31, 1984
Decision Date March 12, 1984
Days to Decision 41 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
74d faster than avg
Panel avg: 115d · This submission: 41d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -