Cleared Traditional

K810836 - DECALCIFIER II (FDA 510(k) Clearance)

Class I Pathology device.

K810836 · Surgipath · Pathology device
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Apr 1981
Decision
28d
Days
Class 1
Risk

K810836 is an FDA 510(k) clearance for the DECALCIFIER II. Classified as Solution, Decalcifier, Acid Containing (product code KDX), Class I - General Controls.

Submitted by Surgipath (Mchenry, US). The FDA issued a Cleared decision on April 23, 1981 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 864.4010 - 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 devices

Submission Details

510(k) Number K810836 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 1981
Decision Date April 23, 1981
Days to Decision 28 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 77d · This submission: 28d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KDX Solution, Decalcifier, Acid Containing
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.4010
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.