Cleared Traditional

K973941 - IMMUNOWELL EBNA IGG TEST

K973941 is an FDA 510(k) clearance for IMMUNOWELL EBNA IGG TEST, manufactured by Genbio. The device is a Class 1 Microbiology device with product code LLM cleared through the Traditional 510(k) pathway after a 299-day FDA review.

K973941 · Genbio · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1998
Decision
299d
Days
Class 1
Risk

K973941 is an FDA 510(k) clearance for the IMMUNOWELL EBNA IGG TEST. Classified as Test, Antigen, Nuclear, Epstein-barr Virus (product code LLM), Class I - General Controls.

Submitted by Genbio (San Diego, US). The FDA issued a Cleared decision on August 10, 1998 after a review of 299 days - an extended review cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3235 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Genbio devices

FDA 510(k) Submission Details - K973941

510(k) Number K973941 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 15, 1997
Decision Date August 10, 1998
Days to Decision 299 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
197d slower than avg
Panel avg: 102d · This submission: 299d
Pathway characteristics
Predicate-based equivalence.

LLM Device Classification - Class 1, General Controls

Product Code LLM Test, Antigen, Nuclear, Epstein-barr Virus
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3235
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.

Regulatory Peers - LLM Test, Antigen, Nuclear, Epstein-barr Virus

All 19
Devices cleared under the same product code (LLM) and FDA review panel - the closest regulatory comparables to K973941.
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