Cleared Traditional

K852014 - EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA (FDA 510(k) Clearance)

Class I Gastroenterology & Urology device.

K852014 · Effner and Spreine Co. · Gastroenterology & Urology device
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Aug 1985
Decision
90d
Days
Class 1
Risk

K852014 is an FDA 510(k) clearance for the EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA. Classified as Surgical Instruments, G-u, Manual (and Accessories) (product code KOA), Class I - General Controls.

Submitted by Effner and Spreine Co. (Port Washington, US). The FDA issued a Cleared decision on August 7, 1985 after a review of 90 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Effner and Spreine Co. devices

Submission Details

510(k) Number K852014 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 09, 1985
Decision Date August 07, 1985
Days to Decision 90 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
40d faster than avg
Panel avg: 130d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KOA Surgical Instruments, G-u, Manual (and Accessories)
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.