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FDA 510(k)

G-TRAINER MEDICAL

K-Number: K072887 · 2008-01-25

ApplicantAlter-G, Inc.
Decision Date2008-01-25
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

G-TRAINER MEDICAL is the device name listed in this FDA 510(k) record. The listed applicant is Alter-G, Inc.. It received FDA 510(k) clearance on 2008-01-25 under 510(k) number K072887. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-TRAINER MEDICAL?

G-TRAINER MEDICAL is a medical device that received FDA 510(k) clearance on 2008-01-25. The listed applicant is Alter-G, Inc.. The 510(k) number is K072887.

When did G-TRAINER MEDICAL receive FDA 510(k) clearance?

G-TRAINER MEDICAL received FDA 510(k) clearance on 2008-01-25, under 510(k) number K072887.

Who is the listed applicant for G-TRAINER MEDICAL?

The FDA 510(k) record lists Alter-G, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G-TRAINER MEDICAL?

The FDA product code for G-TRAINER MEDICAL is BXB.

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Related Devices (Code: BXB)

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

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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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