Cleared Traditional

K852127 - AMSCO URO-ENDO MOBILE TABLE (FDA 510(k) Clearance)

Class I Gastroenterology & Urology device.

K852127 · American Sterilizer Co. · Gastroenterology & Urology device
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Aug 1985
Decision
85d
Days
Class 1
Risk

K852127 is an FDA 510(k) clearance for the AMSCO URO-ENDO MOBILE TABLE. Classified as Table, Cystometric, Non-electric And Accessories (product code KQS), Class I - General Controls.

Submitted by American Sterilizer Co. (Erie, US). The FDA issued a Cleared decision on August 8, 1985 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4890 - 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: 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 American Sterilizer Co. devices

Submission Details

510(k) Number K852127 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 1985
Decision Date August 08, 1985
Days to Decision 85 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
45d faster than avg
Panel avg: 130d · This submission: 85d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KQS Table, Cystometric, Non-electric And Accessories
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.4890
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.