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FDA 510(k)

ARTERIAL/VENOUS BLOODLINES

K-Number: K901688 · 1990-08-02

Decision Date1990-08-02
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARTERIAL/VENOUS BLOODLINES is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1990-08-02 under 510(k) number K901688. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL/VENOUS BLOODLINES?

ARTERIAL/VENOUS BLOODLINES is a medical device that received FDA 510(k) clearance on 1990-08-02. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K901688.

When did ARTERIAL/VENOUS BLOODLINES receive FDA 510(k) clearance?

ARTERIAL/VENOUS BLOODLINES received FDA 510(k) clearance on 1990-08-02, under 510(k) number K901688.

Who is the listed applicant for ARTERIAL/VENOUS BLOODLINES?

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

What is the FDA product code for ARTERIAL/VENOUS BLOODLINES?

The FDA product code for ARTERIAL/VENOUS BLOODLINES is FJK.

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.

Other records listing National Medical Care, Medical Products Div., 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.

View all 62 devices →

Related Devices (Code: FJK)

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

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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