VERTICAL LIFT
K-Number: K983526 · 1998-12-11
Advertisement
Device Summary
Frequently Asked Questions
What is the VERTICAL LIFT?
VERTICAL LIFT is a medical device that received FDA 510(k) clearance on 1998-12-11. The listed applicant is Barnes,Richardson & Colburn. The 510(k) number is K983526.
When did VERTICAL LIFT receive FDA 510(k) clearance?
VERTICAL LIFT received FDA 510(k) clearance on 1998-12-11, under 510(k) number K983526.
Who is the listed applicant for VERTICAL LIFT?
The FDA 510(k) record lists Barnes,Richardson & Colburn as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERTICAL LIFT?
The FDA product code for VERTICAL 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.
Other records listing Barnes,Richardson & Colburn as applicant
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