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FDA 510(k)

ACTIVATOR II

K-Number: K973506 · 1998-01-27

ApplicantActivator Methods, Inc.
Decision Date1998-01-27
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

ACTIVATOR II is the device name listed in this FDA 510(k) record. The listed applicant is Activator Methods, Inc.. It received FDA 510(k) clearance on 1998-01-27 under 510(k) number K973506. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVATOR II?

ACTIVATOR II is a medical device that received FDA 510(k) clearance on 1998-01-27. The listed applicant is Activator Methods, Inc.. The 510(k) number is K973506.

When did ACTIVATOR II receive FDA 510(k) clearance?

ACTIVATOR II received FDA 510(k) clearance on 1998-01-27, under 510(k) number K973506.

Who is the listed applicant for ACTIVATOR II?

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

What is the FDA product code for ACTIVATOR II?

The FDA product code for ACTIVATOR II is LXM.

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Related Devices (Code: LXM)

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.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

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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