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FDA 510(k)

JOHNSON & JOHNSON TUBE SECUREMENT DEVICE

K-Number: K895431 · 1989-10-13

ApplicantJohnson & Johnson Patient Care, Inc.
Decision Date1989-10-13
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON TUBE SECUREMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Patient Care, Inc.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K895431. 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 JOHNSON & JOHNSON TUBE SECUREMENT DEVICE?

JOHNSON & JOHNSON TUBE SECUREMENT DEVICE is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Johnson & Johnson Patient Care, Inc.. The 510(k) number is K895431.

When did JOHNSON & JOHNSON TUBE SECUREMENT DEVICE receive FDA 510(k) clearance?

JOHNSON & JOHNSON TUBE SECUREMENT DEVICE received FDA 510(k) clearance on 1989-10-13, under 510(k) number K895431.

Who is the listed applicant for JOHNSON & JOHNSON TUBE SECUREMENT DEVICE?

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

What is the FDA product code for JOHNSON & JOHNSON TUBE SECUREMENT DEVICE?

The FDA product code for JOHNSON & JOHNSON TUBE SECUREMENT DEVICE is KMK.

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Other records listing Johnson & Johnson Patient Care, 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.

K892851ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVERK890545NU-DERM HYDROCOLLOID DRESSINGK884749JOHNSON & JOHNSON STERILE SPRAY TIP SYRINGE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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