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FDA 510(k)

ASSISTO ARM SYSTEMS

K-Number: K052745 · 2005-11-23

ApplicantGeomed Medizin-Technik GmbH & Co.
Decision Date2005-11-23
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ASSISTO ARM SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Geomed Medizin-Technik GmbH & Co.. It received FDA 510(k) clearance on 2005-11-23 under 510(k) number K052745. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSISTO ARM SYSTEMS?

ASSISTO ARM SYSTEMS is a medical device that received FDA 510(k) clearance on 2005-11-23. The listed applicant is Geomed Medizin-Technik GmbH & Co.. The 510(k) number is K052745.

When did ASSISTO ARM SYSTEMS receive FDA 510(k) clearance?

ASSISTO ARM SYSTEMS received FDA 510(k) clearance on 2005-11-23, under 510(k) number K052745.

Who is the listed applicant for ASSISTO ARM SYSTEMS?

The FDA 510(k) record lists Geomed Medizin-Technik GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASSISTO ARM SYSTEMS?

The FDA product code for ASSISTO ARM SYSTEMS is GWG.

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.

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Other records listing Geomed Medizin-Technik GmbH & Co. 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.

K183438Geomed Vascular Dilators

Related Devices (Code: GWG)

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.

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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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