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FDA 510(k)

ACUBEAM, SUPER NOVA, DIO

K-Number: K022888 · 2002-12-11

ApplicantLight Force Therapy, Inc.
Decision Date2002-12-11
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACUBEAM, SUPER NOVA, DIO is the device name listed in this FDA 510(k) record. The listed applicant is Light Force Therapy, Inc.. It received FDA 510(k) clearance on 2002-12-11 under 510(k) number K022888. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUBEAM, SUPER NOVA, DIO?

ACUBEAM, SUPER NOVA, DIO is a medical device that received FDA 510(k) clearance on 2002-12-11. The listed applicant is Light Force Therapy, Inc.. The 510(k) number is K022888.

When did ACUBEAM, SUPER NOVA, DIO receive FDA 510(k) clearance?

ACUBEAM, SUPER NOVA, DIO received FDA 510(k) clearance on 2002-12-11, under 510(k) number K022888.

Who is the listed applicant for ACUBEAM, SUPER NOVA, DIO?

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

What is the FDA product code for ACUBEAM, SUPER NOVA, DIO?

The FDA product code for ACUBEAM, SUPER NOVA, DIO is ILY.

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 Light Force Therapy, Inc. 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.

K001179SUPER NOVA, ACUBEAM

Related Devices (Code: ILY)

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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