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FDA 510(k)

GARAVENTA SUPER-TRAC TRE-52

K-Number: K020933 · 2002-04-04

Decision Date2002-04-04
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GARAVENTA SUPER-TRAC TRE-52 is the device name listed in this FDA 510(k) record. The listed applicant is Garaventa Accessibility. It received FDA 510(k) clearance on 2002-04-04 under 510(k) number K020933. 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 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

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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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