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FDA 510(k)

LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)

K-Number: K883980 · 1988-12-05

ApplicantMenlo Care, Inc.
Decision Date1988-12-05
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) is the device name listed in this FDA 510(k) record. The listed applicant is Menlo Care, Inc.. It received FDA 510(k) clearance on 1988-12-05 under 510(k) number K883980. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)?

LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Menlo Care, Inc.. The 510(k) number is K883980.

When did LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) receive FDA 510(k) clearance?

LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) received FDA 510(k) clearance on 1988-12-05, under 510(k) number K883980.

Who is the listed applicant for LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)?

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

What is the FDA product code for LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)?

The FDA product code for LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) is FOZ.

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Other records listing Menlo Care, Inc. as applicant

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Related Devices (Code: FOZ)

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.

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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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