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FDA 510(k)

ADHESIVE I.V. CATHETER DRESSING

K-Number: K810579 · 1981-03-26

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1981-03-26
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADHESIVE I.V. CATHETER DRESSING 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 1981-03-26 under 510(k) number K810579. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADHESIVE I.V. CATHETER DRESSING?

ADHESIVE I.V. CATHETER DRESSING is a medical device that received FDA 510(k) clearance on 1981-03-26. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K810579.

When did ADHESIVE I.V. CATHETER DRESSING receive FDA 510(k) clearance?

ADHESIVE I.V. CATHETER DRESSING received FDA 510(k) clearance on 1981-03-26, under 510(k) number K810579.

Who is the listed applicant for ADHESIVE I.V. CATHETER DRESSING?

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 ADHESIVE I.V. CATHETER DRESSING?

The FDA product code for ADHESIVE I.V. CATHETER DRESSING is KMK.

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

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Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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