Cleared Traditional

K850634 - SURGIDYNE SURGIFLO C.W.S. DRAIN PRODUCTS (FDA 510(k) Clearance)

Class I General & Plastic Surgery device.

K850634 · Surgidyne, Inc. · General & Plastic Surgery device
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Jun 1985
Decision
129d
Days
Class 1
Risk

K850634 is an FDA 510(k) clearance for the SURGIDYNE SURGIFLO C.W.S. DRAIN PRODUCTS. Classified as Apparatus, Suction, Single Patient Use, Portable, Nonpowered (product code GCY), Class I - General Controls.

Submitted by Surgidyne, Inc. (Minneapolis, US). The FDA issued a Cleared decision on June 28, 1985 after a review of 129 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4680 - the FDA general and plastic surgery 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Surgidyne, Inc. devices

Submission Details

510(k) Number K850634 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 19, 1985
Decision Date June 28, 1985
Days to Decision 129 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
15d slower than avg
Panel avg: 114d · This submission: 129d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4680
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.