Cleared Traditional

ZETA-SERA D (K812329) - FDA 510(k) Clearance

Class I Microbiology device.

K812329 · Amf Biological and Diagnostics Co. · Microbiology device
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Sep 1981
Decision
14d
Days
Class 1
Risk

K812329 is an FDA 510(k) clearance for the ZETA-SERA D. Classified as Sera, Animal And Human (product code KIS), Class I - General Controls.

Submitted by Amf Biological and Diagnostics Co. (Mchenry, US). The FDA issued a Cleared decision on September 1, 1981 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 864.2800 - the FDA microbiology 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 Amf Biological and Diagnostics Co. devices

Submission Details

510(k) Number K812329 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 1981
Decision Date September 01, 1981
Days to Decision 14 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 102d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KIS Sera, Animal And Human
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.2800
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.