TRUS<T>LIFT PORCH LIFT
K-Number: K964134 · 1996-12-31
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement