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FDA 510(k)

DUOTIP-TEST

K-Number: K941820 · 1994-09-02

ApplicantLincoln Diagnostics, Inc.
Decision Date1994-09-02
Product CodeSCL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUOTIP-TEST is the device name listed in this FDA 510(k) record. The listed applicant is Lincoln Diagnostics, Inc.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K941820. The device is classified under product code SCL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOTIP-TEST?

DUOTIP-TEST is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Lincoln Diagnostics, Inc.. The 510(k) number is K941820.

When did DUOTIP-TEST receive FDA 510(k) clearance?

DUOTIP-TEST received FDA 510(k) clearance on 1994-09-02, under 510(k) number K941820.

Who is the listed applicant for DUOTIP-TEST?

The FDA 510(k) record lists Lincoln Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUOTIP-TEST?

The FDA product code for DUOTIP-TEST is SCL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Lincoln Diagnostics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K961918MULTI-TEST II

Related Devices (Code: SCL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250983Medblue Skin Prick Test Applicator (AS103, AS108, AS109, AS110, AS111, AS113, AS132, AS134, AS146, AS148, AS160, AS162, AS170, AS172)Asistan MedikalK222385Bifurcated NeedleAnhui Tiankang Medical Technology Co., Ltd.K182582Oryum and Ovem Epidermal Deri Prick Test ApplicatorAllergy & Applicator Depot, LLCK172062AllergiEnd ST-9 Multiple Skin Test Applicator, AllergiEnd ST-9 Multiple Well Test TrayMedscience Science Research Group, Inc.K162917Allerhope Allergy Skin TesterProcare Industrial Co., LimitedK032528BD ECLIPSE BIFURCATED NEEDLEBecton, Dickinson & CO

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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