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FDA 510(k)

MEDICOTEST SKIN FIX

K-Number: K926264 · 1993-04-20

ApplicantMedicotest, Inc.
Decision Date1993-04-20
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICOTEST SKIN FIX is the device name listed in this FDA 510(k) record. The listed applicant is Medicotest, Inc.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K926264. 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 MEDICOTEST SKIN FIX?

MEDICOTEST SKIN FIX is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Medicotest, Inc.. The 510(k) number is K926264.

When did MEDICOTEST SKIN FIX receive FDA 510(k) clearance?

MEDICOTEST SKIN FIX received FDA 510(k) clearance on 1993-04-20, under 510(k) number K926264.

Who is the listed applicant for MEDICOTEST SKIN FIX?

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

What is the FDA product code for MEDICOTEST SKIN FIX?

The FDA product code for MEDICOTEST SKIN FIX is KGX.

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Other records listing Medicotest, 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.

K983597NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODESK970639NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-KK961643MEDICOTEST ECG ELECTRODESK952176DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-KK941568K-10-VS, DA-05-VS, RECORDING ELECTRODESK931426NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE

View all 14 devices →

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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