Cleared Traditional

ASPIRATING AND IRRIGATING CYSTS NEEDLES (K885283) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K885283 · Go Medical Industries Pty. , Ltd. · General & Plastic Surgery device
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Mar 1989
Decision
92d
Days
Class 1
Risk

K885283 is an FDA 510(k) clearance for the ASPIRATING AND IRRIGATING CYSTS NEEDLES. Classified as Needle, Aspiration And Injection, Reusable (product code GDM), Class I - General Controls.

Submitted by Go Medical Industries Pty. , Ltd. (Western Australia, AU). The FDA issued a Cleared decision on March 22, 1989 after a review of 92 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 Go Medical Industries Pty. , Ltd. devices

Submission Details

510(k) Number K885283 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 20, 1988
Decision Date March 22, 1989
Days to Decision 92 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
23d faster than avg
Panel avg: 115d · This submission: 92d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GDM Needle, Aspiration And Injection, Reusable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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.