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FDA 510(k)

CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY

K-Number: K901374 · 1990-06-26

ApplicantMenlo Care, Inc.
Decision Date1990-06-26
Product Code
DecisionUnknown

Device Summary

CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY 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 1990-06-26 under 510(k) number K901374. FDA Decision: Unknown.

Frequently Asked Questions

What is the CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY?

CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is Menlo Care, Inc.. The 510(k) number is K901374.

When did CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY receive FDA 510(k) clearance?

CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY received FDA 510(k) clearance on 1990-06-26, under 510(k) number K901374.

Who is the listed applicant for CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY?

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

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Other records listing Menlo 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.

K964447PICC CATHETER/MIDLINE CATHETERK951620MIDMARK MIDLINE CATHETERK945521CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAYK950737LANDMARK MIDLINE CATHETERK944968LANDMARK MIDLINE CATHETERK943893PERCUTANEOUS GRAINAGE CATHETER

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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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