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FDA 510(k)

BAND-AID BRAND TRICOT MESH BANDAGES

K-Number: K801823 · 1980-08-20

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1980-08-20
Product CodeKGY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BAND-AID BRAND TRICOT MESH 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 1980-08-20 under 510(k) number K801823. The device is classified under product code KGY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAND-AID BRAND TRICOT MESH BANDAGES?

BAND-AID BRAND TRICOT MESH BANDAGES is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K801823.

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

BAND-AID BRAND TRICOT MESH BANDAGES received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801823.

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

The FDA product code for BAND-AID BRAND TRICOT MESH BANDAGES is KGY.

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

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Related Devices (Code: KGY)

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.

K933085GOODMAN BANDAGEMegadyne Medical Products, Inc.K913678TROCAR CATHETERMedovations, Inc.K910914SURGICAL TISSUE POUCHCook Urological, Inc.K832318ISOLATION BAG 3M3M CompanyK801824BAND-AID BRAND FLEXIBLE FABRIC BANDAGEJohnson & Johnson Professionals, 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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