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FDA 510(k)

BAND-AID BRAND SHEER BANDAGES

K-Number: K761335 · 1977-01-05

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1977-01-05
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAND-AID BRAND SHEER BANDAGES is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761335. 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 BAND-AID BRAND SHEER BANDAGES?

BAND-AID BRAND SHEER BANDAGES is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K761335.

When did BAND-AID BRAND SHEER BANDAGES receive FDA 510(k) clearance?

BAND-AID BRAND SHEER BANDAGES received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761335.

Who is the listed applicant for BAND-AID BRAND SHEER BANDAGES?

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

What is the FDA product code for BAND-AID BRAND SHEER BANDAGES?

The FDA product code for BAND-AID BRAND SHEER BANDAGES is KGX.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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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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