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FDA 510(k)

BIOCLUSIVE MVP TRANSPARENT DRESSING

K-Number: K923235 · 1993-05-12

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1993-05-12
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIOCLUSIVE MVP TRANSPARENT DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K923235. 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 BIOCLUSIVE MVP TRANSPARENT DRESSING?

BIOCLUSIVE MVP TRANSPARENT DRESSING is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K923235.

When did BIOCLUSIVE MVP TRANSPARENT DRESSING receive FDA 510(k) clearance?

BIOCLUSIVE MVP TRANSPARENT DRESSING received FDA 510(k) clearance on 1993-05-12, under 510(k) number K923235.

Who is the listed applicant for BIOCLUSIVE MVP TRANSPARENT DRESSING?

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

What is the FDA product code for BIOCLUSIVE MVP TRANSPARENT DRESSING?

The FDA product code for BIOCLUSIVE MVP TRANSPARENT DRESSING is KGX.

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Other records listing Johnson & Johnson Medical, 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.

K001690PROTECTIV SAFETY BLOOD COLLECTION NEEDLEK982641ADVANCED NIBP MODULEK983362NU-GEL * WOUND DRESSINGK982597FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATEK974080CRITIKON SOFT BLOOD PRESSURE CUFFK980493I.V. CATHETER SYSTEM

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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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