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FDA 510(k)

LC STRIP

K-Number: K923358 · 1993-01-13

ApplicantGenetic Laboratories Wound Care, Inc.
Decision Date1993-01-13
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LC STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Genetic Laboratories Wound Care, Inc.. It received FDA 510(k) clearance on 1993-01-13 under 510(k) number K923358. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LC STRIP?

LC STRIP is a medical device that received FDA 510(k) clearance on 1993-01-13. The listed applicant is Genetic Laboratories Wound Care, Inc.. The 510(k) number is K923358.

When did LC STRIP receive FDA 510(k) clearance?

LC STRIP received FDA 510(k) clearance on 1993-01-13, under 510(k) number K923358.

Who is the listed applicant for LC STRIP?

The FDA 510(k) record lists Genetic Laboratories Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LC STRIP?

The FDA product code for LC STRIP is KGX.

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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