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FDA 510(k)

TRIFIT 700

K-Number: K033646 · 2005-03-01

ApplicantHealthfirst Corp.
Decision Date2005-03-01
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRIFIT 700 is the device name listed in this FDA 510(k) record. The listed applicant is Healthfirst Corp.. It received FDA 510(k) clearance on 2005-03-01 under 510(k) number K033646. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIFIT 700?

TRIFIT 700 is a medical device that received FDA 510(k) clearance on 2005-03-01. The listed applicant is Healthfirst Corp.. The 510(k) number is K033646.

When did TRIFIT 700 receive FDA 510(k) clearance?

TRIFIT 700 received FDA 510(k) clearance on 2005-03-01, under 510(k) number K033646.

Who is the listed applicant for TRIFIT 700?

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

What is the FDA product code for TRIFIT 700?

The FDA product code for TRIFIT 700 is DRT.

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Related Devices (Code: DRT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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