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FDA 510(k)

ACTIBAND

K-Number: K022404 · 2002-08-08

ApplicantPaw, LLC
Decision Date2002-08-08
Product CodeILX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTIBAND is the device name listed in this FDA 510(k) record. The listed applicant is Paw, LLC. It received FDA 510(k) clearance on 2002-08-08 under 510(k) number K022404. The device is classified under product code ILX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIBAND?

ACTIBAND is a medical device that received FDA 510(k) clearance on 2002-08-08. The listed applicant is Paw, LLC. The 510(k) number is K022404.

When did ACTIBAND receive FDA 510(k) clearance?

ACTIBAND received FDA 510(k) clearance on 2002-08-08, under 510(k) number K022404.

Who is the listed applicant for ACTIBAND?

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

What is the FDA product code for ACTIBAND?

The FDA product code for ACTIBAND is ILX.

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Related Devices (Code: ILX)

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.

K241395Active System; Avenue8Caerus CorporationK202337Pulsed electromagnetic field wrapHi-Dow International, Inc.K190251RecoveryRxBioelectronics CorporationK131979PROVANT THERAPY SYSTEMRegenesis Biomedical, Inc.K121702ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICEOrthocor MedicalK121338ZEOBIIvivi Health Science, LLC

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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