Cleared Traditional

K864495 - MEDSURG VASCULAR ACCESS PORT INFUSION TRAY (FDA 510(k) Clearance)

K864495 · Medsurg Industries, Inc. · General & Plastic Surgery device
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Dec 1986
Decision
46d
Days
-
Risk

K864495 is an FDA 510(k) clearance for the MEDSURG VASCULAR ACCESS PORT INFUSION TRAY.

Submitted by Medsurg Industries, Inc. (Herndon, US). The FDA issued a Cleared decision on December 30, 1986 after a review of 46 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery 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 Medsurg Industries, Inc. devices

Submission Details

510(k) Number K864495 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1986
Decision Date December 30, 1986
Days to Decision 46 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 114d · This submission: 46d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -