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FDA 510(k)

THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY

K-Number: K851495 · 1985-08-01

ApplicantThoratec Laboratories Corp.
Decision Date1985-08-01
Product Code
DecisionUnknown

Device Summary

THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Thoratec Laboratories Corp.. It received FDA 510(k) clearance on 1985-08-01 under 510(k) number K851495. FDA Decision: Unknown.

Frequently Asked Questions

What is the THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY?

THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY is a medical device that received FDA 510(k) clearance on 1985-08-01. The listed applicant is Thoratec Laboratories Corp.. The 510(k) number is K851495.

When did THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY receive FDA 510(k) clearance?

THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY received FDA 510(k) clearance on 1985-08-01, under 510(k) number K851495.

Who is the listed applicant for THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY?

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

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Other records listing Thoratec Laboratories Corp. 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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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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