Multi-Test PC Skin Test System

Multiple head skin test applicator for allergy testing, case of 600.

Registry build 21.09.26
4manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Anhui (1), Henan (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code SCL
Manufacturer City Province Registered as Device types
Dongguan Shun King Company Limited Dongguan Guangdong Contract manufacturer 4
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Anhui Tiankang Medical Technology Co., Ltd. Tianchang Anhui Contract manufacturer 9
Procare Industrial Co., Limited Zhengzhou Henan Manufacturer 3

Record

Regulatory record for Multi-Test PC Skin Test System
Listed by Lincoln Diagnostics, Inc., United States
FDA product code SCL
Device type Allergen And Vaccine Delivery Needles
Device class Class 2
Regulation 21 CFR 880.5570
Establishment Manufacturer
510(k) K961918
Record published 2025-12-12

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Multi-Test PC Skin Test System
Catalogue number Size Per pack Status
MH-6 PC 6 In distribution
MH-BLK PC 600 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Multi-Test II Skin Test System Lincoln Diagnostics, Inc. 2
Multi-Test Skin Test System Lincoln Diagnostics, Inc. 2
Duotip-Test Skin Test System Lincoln Diagnostics, Inc. 1
Multi-Test Dipwell Tray, non-capped Lincoln Diagnostics, Inc. 1
Duotip-Test Dipwell Tray Lincoln Diagnostics, Inc. 1
Duotip-Test II Skin Test System Lincoln Diagnostics, Inc. 1
Wells for Pyramid Dipwell Tray Lincoln Diagnostics, Inc. 1
UniTest PC Skin Test System Lincoln Diagnostics, Inc. 1
Multi-Test Dipwell Tray Lincoln Diagnostics, Inc. 1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K961918 1996-08-07
K941820 1994-09-02

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer