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FDA 510(k)

THORA-KLEX AUTOTRANSFUSION KIT

K-Number: K843586 · 1984-10-25

ApplicantC.R. Bard, Inc.
Decision Date1984-10-25
Product Code
DecisionSubstantially Equivalent

Device Summary

THORA-KLEX AUTOTRANSFUSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K843586. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORA-KLEX AUTOTRANSFUSION KIT?

THORA-KLEX AUTOTRANSFUSION KIT is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K843586.

When did THORA-KLEX AUTOTRANSFUSION KIT receive FDA 510(k) clearance?

THORA-KLEX AUTOTRANSFUSION KIT received FDA 510(k) clearance on 1984-10-25, under 510(k) number K843586.

Who is the listed applicant for THORA-KLEX AUTOTRANSFUSION KIT?

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

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Other records listing C.R. Bard, 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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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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