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FDA 510(k)

DVT60

K-Number: K022786 · 2002-09-19

ApplicantHuntleigh Healthcare, Inc.
Decision Date2002-09-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DVT60 is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Healthcare, Inc.. It received FDA 510(k) clearance on 2002-09-19 under 510(k) number K022786. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVT60?

DVT60 is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is Huntleigh Healthcare, Inc.. The 510(k) number is K022786.

When did DVT60 receive FDA 510(k) clearance?

DVT60 received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022786.

Who is the listed applicant for DVT60?

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

What is the FDA product code for DVT60?

The FDA product code for DVT60 is JOW.

Other records listing Huntleigh Healthcare, Inc. as applicant

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Related Devices (Code: JOW)

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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