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FDA 510(k)

MCPARLAND SCALP VEIN CATHETER

K-Number: K821001 · 1982-07-22

Decision Date1982-07-22
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MCPARLAND SCALP VEIN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Renal Systems, Inc.. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K821001. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCPARLAND SCALP VEIN CATHETER?

MCPARLAND SCALP VEIN CATHETER is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Renal Systems, Inc.. The 510(k) number is K821001.

When did MCPARLAND SCALP VEIN CATHETER receive FDA 510(k) clearance?

MCPARLAND SCALP VEIN CATHETER received FDA 510(k) clearance on 1982-07-22, under 510(k) number K821001.

Who is the listed applicant for MCPARLAND SCALP VEIN CATHETER?

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

What is the FDA product code for MCPARLAND SCALP VEIN CATHETER?

The FDA product code for MCPARLAND SCALP VEIN CATHETER is LFJ.

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 Renal Systems, 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.

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Related Devices (Code: LFJ)

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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