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FDA 510(k)

DEVMED STEPPING AND STABILIZING SYSTEM

K-Number: K972152 · 1997-08-15

ApplicantDevmed Corp.
Decision Date1997-08-15
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DEVMED STEPPING AND STABILIZING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Devmed Corp.. It received FDA 510(k) clearance on 1997-08-15 under 510(k) number K972152. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVMED STEPPING AND STABILIZING SYSTEM?

DEVMED STEPPING AND STABILIZING SYSTEM is a medical device that received FDA 510(k) clearance on 1997-08-15. The listed applicant is Devmed Corp.. The 510(k) number is K972152.

When did DEVMED STEPPING AND STABILIZING SYSTEM receive FDA 510(k) clearance?

DEVMED STEPPING AND STABILIZING SYSTEM received FDA 510(k) clearance on 1997-08-15, under 510(k) number K972152.

Who is the listed applicant for DEVMED STEPPING AND STABILIZING SYSTEM?

The FDA 510(k) record lists Devmed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVMED STEPPING AND STABILIZING SYSTEM?

The FDA product code for DEVMED STEPPING AND STABILIZING SYSTEM is ITX.

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 Devmed Corp. 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: ITX)

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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