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FDA 510(k)

LACTOFERRIN MICROASSAY SYSTEM

K-Number: K934473 · 1993-12-03

ApplicantTouch Scientific, Inc.
Decision Date1993-12-03
Product CodeDEG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LACTOFERRIN MICROASSAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Touch Scientific, Inc.. It received FDA 510(k) clearance on 1993-12-03 under 510(k) number K934473. The device is classified under product code DEG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTOFERRIN MICROASSAY SYSTEM?

LACTOFERRIN MICROASSAY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-12-03. The listed applicant is Touch Scientific, Inc.. The 510(k) number is K934473.

When did LACTOFERRIN MICROASSAY SYSTEM receive FDA 510(k) clearance?

LACTOFERRIN MICROASSAY SYSTEM received FDA 510(k) clearance on 1993-12-03, under 510(k) number K934473.

Who is the listed applicant for LACTOFERRIN MICROASSAY SYSTEM?

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

What is the FDA product code for LACTOFERRIN MICROASSAY SYSTEM?

The FDA product code for LACTOFERRIN MICROASSAY SYSTEM is DEG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Touch Scientific, 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.

K991316TOUCH TEAR IGE MICROASSAY KITK931901LACTOCARD

Related Devices (Code: DEG)

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.

K071712LEUKO EZ VUETechlab Inc., Corporate Research CenterK042071IBD-SCANTechlab, Inc.K030704IBD-QUIK CHEKTechlab, Inc.K011396IBD-CHEKTechlab, Inc.K951101LEUKO-TESTTechlab, Inc.K931901LACTOCARDTouch Scientific, Inc.

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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