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FDA 510(k)

TRUS<T>LIFT PORCH LIFT

K-Number: K964134 · 1996-12-31

ApplicantTrus T Lift
Decision Date1996-12-31
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRUS<T>LIFT PORCH LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Trus T Lift. It received FDA 510(k) clearance on 1996-12-31 under 510(k) number K964134. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUS<T>LIFT PORCH LIFT?

TRUS<T>LIFT PORCH LIFT is a medical device that received FDA 510(k) clearance on 1996-12-31. The listed applicant is Trus T Lift. The 510(k) number is K964134.

When did TRUS<T>LIFT PORCH LIFT receive FDA 510(k) clearance?

TRUS<T>LIFT PORCH LIFT received FDA 510(k) clearance on 1996-12-31, under 510(k) number K964134.

Who is the listed applicant for TRUS<T>LIFT PORCH LIFT?

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

What is the FDA product code for TRUS<T>LIFT PORCH LIFT?

The FDA product code for TRUS<T>LIFT PORCH LIFT is ING.

Related Clinical Trials

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.

Related Devices (Code: ING)

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.

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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