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FDA 510(k)

IMAGEQUEST

K-Number: K974707 · 1998-07-31

ApplicantVisual Med, Inc.
Decision Date1998-07-31
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGEQUEST is the device name listed in this FDA 510(k) record. The listed applicant is Visual Med, Inc.. It received FDA 510(k) clearance on 1998-07-31 under 510(k) number K974707. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGEQUEST?

IMAGEQUEST is a medical device that received FDA 510(k) clearance on 1998-07-31. The listed applicant is Visual Med, Inc.. The 510(k) number is K974707.

When did IMAGEQUEST receive FDA 510(k) clearance?

IMAGEQUEST received FDA 510(k) clearance on 1998-07-31, under 510(k) number K974707.

Who is the listed applicant for IMAGEQUEST?

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

What is the FDA product code for IMAGEQUEST?

The FDA product code for IMAGEQUEST is LMD.

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Related Devices (Code: LMD)

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.

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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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