Cleared Traditional

K070763 - EUROIMMUN ANA IFA: HEP-20-10

K070763 is an FDA 510(k) clearance for EUROIMMUN ANA IFA: HEP-20-10, manufactured by Euroimmun Us, LLC. The device is a Class 2 Immunology device with product code DHN cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K070763 · Euroimmun Us, LLC · Immunology device
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May 2007
Decision
63d
Days
Class 2
Risk

K070763 is an FDA 510(k) clearance for the EUROIMMUN ANA IFA: HEP-20-10. Classified as Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control (product code DHN), Class II - Special Controls.

Submitted by Euroimmun Us, LLC (Boonton Township, US). The FDA issued a Cleared decision on May 22, 2007 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5100 - the FDA immunology 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 Euroimmun Us, LLC devices

FDA 510(k) Submission Details - K070763

510(k) Number K070763 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 2007
Decision Date May 22, 2007
Days to Decision 63 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 105d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DHN Device Classification - Class 2, Special Controls

Product Code DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5100
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Immunology devices follow this clearance model.

Regulatory Peers - DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

All 66
Devices cleared under the same product code (DHN) and FDA review panel - the closest regulatory comparables to K070763.
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