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FDA 510(k)

EV APAN DIGITAL, MODEL K1VSM2000

K-Number: K041120 · 2004-08-30

ApplicantAfp Imaging Corp.
Decision Date2004-08-30
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EV APAN DIGITAL, MODEL K1VSM2000 is the device name listed in this FDA 510(k) record. The listed applicant is Afp Imaging Corp.. It received FDA 510(k) clearance on 2004-08-30 under 510(k) number K041120. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EV APAN DIGITAL, MODEL K1VSM2000?

EV APAN DIGITAL, MODEL K1VSM2000 is a medical device that received FDA 510(k) clearance on 2004-08-30. The listed applicant is Afp Imaging Corp.. The 510(k) number is K041120.

When did EV APAN DIGITAL, MODEL K1VSM2000 receive FDA 510(k) clearance?

EV APAN DIGITAL, MODEL K1VSM2000 received FDA 510(k) clearance on 2004-08-30, under 510(k) number K041120.

Who is the listed applicant for EV APAN DIGITAL, MODEL K1VSM2000?

The FDA 510(k) record lists Afp Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EV APAN DIGITAL, MODEL K1VSM2000?

The FDA product code for EV APAN DIGITAL, MODEL K1VSM2000 is MUH.

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Other records listing Afp Imaging Corp. as applicant

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Related Devices (Code: MUH)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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