Cleared Traditional

K800052 - ANTIMICROBIAL REMOVAL DEVICE (ARD) (FDA 510(k) Clearance)

K800052 · Marion Laboratories, Inc. · Microbiology device
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Apr 1980
Decision
86d
Days
-
Risk

K800052 is an FDA 510(k) clearance for the ANTIMICROBIAL REMOVAL DEVICE (ARD).

Submitted by Marion Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 4, 1980 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel. 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 Marion Laboratories, Inc. devices

Submission Details

510(k) Number K800052 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 1980
Decision Date April 04, 1980
Days to Decision 86 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
16d faster than avg
Panel avg: 102d · This submission: 86d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -