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FDA 510(k)

INTRAVASCULAR CATHETER SECUREMENT DEV

K-Number: K841487 · 1984-06-28

ApplicantTapemark Co.
Decision Date1984-06-28
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVASCULAR CATHETER SECUREMENT DEV is the device name listed in this FDA 510(k) record. The listed applicant is Tapemark Co.. It received FDA 510(k) clearance on 1984-06-28 under 510(k) number K841487. 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 INTRAVASCULAR CATHETER SECUREMENT DEV?

INTRAVASCULAR CATHETER SECUREMENT DEV is a medical device that received FDA 510(k) clearance on 1984-06-28. The listed applicant is Tapemark Co.. The 510(k) number is K841487.

When did INTRAVASCULAR CATHETER SECUREMENT DEV receive FDA 510(k) clearance?

INTRAVASCULAR CATHETER SECUREMENT DEV received FDA 510(k) clearance on 1984-06-28, under 510(k) number K841487.

Who is the listed applicant for INTRAVASCULAR CATHETER SECUREMENT DEV?

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

What is the FDA product code for INTRAVASCULAR CATHETER SECUREMENT DEV?

The FDA product code for INTRAVASCULAR CATHETER SECUREMENT DEV is KMK.

Related Clinical Trials

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.

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.

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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