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FDA 510(k)

LOW TRAUMA ARTERIAL FILTER H-640

K-Number: K831507 · 1983-12-29

ApplicantC.R. Bard, Inc.
Decision Date1983-12-29
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LOW TRAUMA ARTERIAL FILTER H-640 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 1983-12-29 under 510(k) number K831507. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW TRAUMA ARTERIAL FILTER H-640?

LOW TRAUMA ARTERIAL FILTER H-640 is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K831507.

When did LOW TRAUMA ARTERIAL FILTER H-640 receive FDA 510(k) clearance?

LOW TRAUMA ARTERIAL FILTER H-640 received FDA 510(k) clearance on 1983-12-29, under 510(k) number K831507.

Who is the listed applicant for LOW TRAUMA ARTERIAL FILTER H-640?

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

What is the FDA product code for LOW TRAUMA ARTERIAL FILTER H-640?

The FDA product code for LOW TRAUMA ARTERIAL FILTER H-640 is DTM.

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Related Devices (Code: DTM)

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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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