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FDA 510(k)

PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION

K-Number: K031372 · 2003-07-02

ApplicantMaxxvision, LLC
Decision Date2003-07-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Maxxvision, LLC. It received FDA 510(k) clearance on 2003-07-02 under 510(k) number K031372. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION?

PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION is a medical device that received FDA 510(k) clearance on 2003-07-02. The listed applicant is Maxxvision, LLC. The 510(k) number is K031372.

When did PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION receive FDA 510(k) clearance?

PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION received FDA 510(k) clearance on 2003-07-02, under 510(k) number K031372.

Who is the listed applicant for PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION?

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

What is the FDA product code for PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION?

The FDA product code for PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION is LLZ.

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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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