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FDA 510(k)

MAXVIEW DIAGNOSTIC WORKSTATION

K-Number: K984023 · 1998-12-08

ApplicantDynamic Healthcare Technologies, Inc.
Decision Date1998-12-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAXVIEW DIAGNOSTIC WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Dynamic Healthcare Technologies, Inc.. It received FDA 510(k) clearance on 1998-12-08 under 510(k) number K984023. 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 MAXVIEW DIAGNOSTIC WORKSTATION?

MAXVIEW DIAGNOSTIC WORKSTATION is a medical device that received FDA 510(k) clearance on 1998-12-08. The listed applicant is Dynamic Healthcare Technologies, Inc.. The 510(k) number is K984023.

When did MAXVIEW DIAGNOSTIC WORKSTATION receive FDA 510(k) clearance?

MAXVIEW DIAGNOSTIC WORKSTATION received FDA 510(k) clearance on 1998-12-08, under 510(k) number K984023.

Who is the listed applicant for MAXVIEW DIAGNOSTIC WORKSTATION?

The FDA 510(k) record lists Dynamic Healthcare Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAXVIEW DIAGNOSTIC WORKSTATION?

The FDA product code for MAXVIEW DIAGNOSTIC 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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