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FDA 510(k)

VARI/MOIST WOUND DRESSING

K-Number: K896358 · 1990-02-01

ApplicantCatalina Biomedical Corp.
Decision Date1990-02-01
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

VARI/MOIST WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Catalina Biomedical Corp.. It received FDA 510(k) clearance on 1990-02-01 under 510(k) number K896358. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the VARI/MOIST WOUND DRESSING?

VARI/MOIST WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1990-02-01. The listed applicant is Catalina Biomedical Corp.. The 510(k) number is K896358.

When did VARI/MOIST WOUND DRESSING receive FDA 510(k) clearance?

VARI/MOIST WOUND DRESSING received FDA 510(k) clearance on 1990-02-01, under 510(k) number K896358.

Who is the listed applicant for VARI/MOIST WOUND DRESSING?

The FDA 510(k) record lists Catalina Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARI/MOIST WOUND DRESSING?

The FDA product code for VARI/MOIST WOUND DRESSING is KGX.

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 Catalina Biomedical Corp. 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.

K920050BIOLEX WOUND GEL,K913480WOUND CARE TRAY AK913479WOUND CARE TRAY BK896421TRANSPARENT FILM I.V. SITE/WOUND DRESSING

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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