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FDA 510(k)

DIGITAL DOC

K-Number: K981663 · 1998-08-10

ApplicantDigital Doc, LLC
Decision Date1998-08-10
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIGITAL DOC is the device name listed in this FDA 510(k) record. The listed applicant is Digital Doc, LLC. It received FDA 510(k) clearance on 1998-08-10 under 510(k) number K981663. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL DOC?

DIGITAL DOC is a medical device that received FDA 510(k) clearance on 1998-08-10. The listed applicant is Digital Doc, LLC. The 510(k) number is K981663.

When did DIGITAL DOC receive FDA 510(k) clearance?

DIGITAL DOC received FDA 510(k) clearance on 1998-08-10, under 510(k) number K981663.

Who is the listed applicant for DIGITAL DOC?

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

What is the FDA product code for DIGITAL DOC?

The FDA product code for DIGITAL DOC is EIA.

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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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