ULTIMATE
K-Number: K920444 · 1992-04-20
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Device Summary
Frequently Asked Questions
What is the ULTIMATE?
ULTIMATE is a medical device that received FDA 510(k) clearance on 1992-04-20. The listed applicant is Jobst Institute, Inc.. The 510(k) number is K920444.
When did ULTIMATE receive FDA 510(k) clearance?
ULTIMATE received FDA 510(k) clearance on 1992-04-20, under 510(k) number K920444.
Who is the listed applicant for ULTIMATE?
The FDA 510(k) record lists Jobst Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTIMATE?
The FDA product code for ULTIMATE is DWL.
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 Jobst Institute, Inc. 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: DWL)
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.
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