Cleared Traditional

MULTI-TEST (K760699) - FDA 510(k) Clearance

Class II Immunology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K760699 · Lincoln Laboratories, Inc. · Immunology device
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Dec 1976
Decision
99d
Days
Class 2
Risk

K760699 is an FDA 510(k) clearance for the MULTI-TEST. Classified as Allergen And Vaccine Delivery Needles (product code SCL), Class II - Special Controls.

Submitted by Lincoln Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 30, 1976 after a review of 99 days - within the typical 510(k) review window.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 880.5570 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Immunology review framework, consistent with the majority of Class II 510(k) submissions.

View all Lincoln Laboratories, Inc. devices

Submission Details

510(k) Number K760699 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 1976
Decision Date December 30, 1976
Days to Decision 99 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
5d faster than avg
Panel avg: 104d · This submission: 99d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code SCL Allergen And Vaccine Delivery Needles
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5570
Definition An Allergen Delivery Needle Is A Device Intended To Percutaneously Deliver Diagnostic Allergenic Extracts For Use In Allergy Skin Tests Also Referred To As Skin Prick Tests Or Intradermal Allergy Tests.
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 - SCL Allergen And Vaccine Delivery Needles

Devices cleared under the same product code (SCL) and FDA review panel - the closest regulatory comparables to K760699.
Oryum and Ovem Epidermal Deri Prick Test Applicator
K182582 · Allergy & Applicator Depot, LLC · Apr 2019
AllergiEnd ST-9 Multiple Skin Test Applicator, AllergiEnd ST-9 Multiple Well Test Tray
K172062 · Medscience Science Research Group, Inc. · Mar 2018
BD ECLIPSE BIFURCATED NEEDLE
K032528 · Becton, Dickinson & CO · Sep 2003