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FDA 510(k)

HEXAPOD RT COUCHTOP

K-Number: K041448 · 2004-06-16

Decision Date2004-06-16
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HEXAPOD RT COUCHTOP is the device name listed in this FDA 510(k) record. The listed applicant is Medical Intelligence Medizintechnik GmbH. It received FDA 510(k) clearance on 2004-06-16 under 510(k) number K041448. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEXAPOD RT COUCHTOP?

HEXAPOD RT COUCHTOP is a medical device that received FDA 510(k) clearance on 2004-06-16. The listed applicant is Medical Intelligence Medizintechnik GmbH. The 510(k) number is K041448.

When did HEXAPOD RT COUCHTOP receive FDA 510(k) clearance?

HEXAPOD RT COUCHTOP received FDA 510(k) clearance on 2004-06-16, under 510(k) number K041448.

Who is the listed applicant for HEXAPOD RT COUCHTOP?

The FDA 510(k) record lists Medical Intelligence Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEXAPOD RT COUCHTOP?

The FDA product code for HEXAPOD RT COUCHTOP is JAI.

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 Medical Intelligence Medizintechnik GmbH 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.

View all 7 devices →

Related Devices (Code: JAI)

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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