GARAVENTA SUPER-TRAC TRE-52
K-Number: K020933 · 2002-04-04
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Device Summary
Frequently Asked Questions
What is the GARAVENTA SUPER-TRAC TRE-52?
GARAVENTA SUPER-TRAC TRE-52 is a medical device that received FDA 510(k) clearance on 2002-04-04. The listed applicant is Garaventa Accessibility. The 510(k) number is K020933.
When did GARAVENTA SUPER-TRAC TRE-52 receive FDA 510(k) clearance?
GARAVENTA SUPER-TRAC TRE-52 received FDA 510(k) clearance on 2002-04-04, under 510(k) number K020933.
Who is the listed applicant for GARAVENTA SUPER-TRAC TRE-52?
The FDA 510(k) record lists Garaventa Accessibility as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GARAVENTA SUPER-TRAC TRE-52?
The FDA product code for GARAVENTA SUPER-TRAC TRE-52 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 Garaventa Accessibility 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.
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