Cleared Traditional

K873889 - TISSUE CULTURE TUBES (FDA 510(k) Clearance)

Class I Pathology device.

K873889 · Nunc, Inc. · Pathology device
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Nov 1987
Decision
63d
Days
Class 1
Risk

K873889 is an FDA 510(k) clearance for the TISSUE CULTURE TUBES. Classified as Flask, Tissue Culture (product code KJA), Class I - General Controls.

Submitted by Nunc, Inc. (Riverside, US). The FDA issued a Cleared decision on November 25, 1987 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 864.2240 - 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 Nunc, Inc. devices

Submission Details

510(k) Number K873889 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1987
Decision Date November 25, 1987
Days to Decision 63 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d faster than avg
Panel avg: 77d · This submission: 63d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KJA Flask, Tissue Culture
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.2240
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.