Cleared Traditional

K831335 - DISPOSABLE BASE MOLD (FDA 510(k) Clearance)

Class I Pathology device.

K831335 · Surgipath Medical Industries, Inc. · Pathology device
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May 1983
Decision
21d
Days
Class 1
Risk

K831335 is an FDA 510(k) clearance for the DISPOSABLE BASE MOLD. Classified as Container, Embedding (product code KER), Class I - General Controls.

Submitted by Surgipath Medical Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 16, 1983 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 864.3010 - the FDA pathology 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 Surgipath Medical Industries, Inc. devices

Submission Details

510(k) Number K831335 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1983
Decision Date May 16, 1983
Days to Decision 21 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 77d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KER Container, Embedding
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.3010
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.