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FDA 510(k)

DERMIVIEW CLEAR TAPE

K-Number: K942383 · 1994-08-22

ApplicantJohnson & Johnson International
Decision Date1994-08-22
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMIVIEW CLEAR TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson International. It received FDA 510(k) clearance on 1994-08-22 under 510(k) number K942383. 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 DERMIVIEW CLEAR TAPE?

DERMIVIEW CLEAR TAPE is a medical device that received FDA 510(k) clearance on 1994-08-22. The listed applicant is Johnson & Johnson International. The 510(k) number is K942383.

When did DERMIVIEW CLEAR TAPE receive FDA 510(k) clearance?

DERMIVIEW CLEAR TAPE received FDA 510(k) clearance on 1994-08-22, under 510(k) number K942383.

Who is the listed applicant for DERMIVIEW CLEAR TAPE?

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

What is the FDA product code for DERMIVIEW CLEAR TAPE?

The FDA product code for DERMIVIEW CLEAR TAPE is KGX.

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Other records listing Johnson & Johnson International 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.

K965198ULTIMA TPS CEMENTED STEMK944937SYNTHETIC ABSORBABLE SUTUREK946245TIELLE* HYDROPOLYMER DRESSINGK922918BARRIER SAF-TE HYDROGEL DRAPEK923807P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUSK896828BIOCLUSIVE(R) ABSORBENT DRESSING

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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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