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FDA 510(k)

EXPERT MORPHOMERTY SOFTWARD

K-Number: K950611 · 1995-05-24

ApplicantLunar Corp.
Decision Date1995-05-24
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EXPERT MORPHOMERTY SOFTWARD is the device name listed in this FDA 510(k) record. The listed applicant is Lunar Corp.. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K950611. The device is classified under product code KGI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPERT MORPHOMERTY SOFTWARD?

EXPERT MORPHOMERTY SOFTWARD is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Lunar Corp.. The 510(k) number is K950611.

When did EXPERT MORPHOMERTY SOFTWARD receive FDA 510(k) clearance?

EXPERT MORPHOMERTY SOFTWARD received FDA 510(k) clearance on 1995-05-24, under 510(k) number K950611.

Who is the listed applicant for EXPERT MORPHOMERTY SOFTWARD?

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

What is the FDA product code for EXPERT MORPHOMERTY SOFTWARD?

The FDA product code for EXPERT MORPHOMERTY SOFTWARD is KGI.

Related Clinical Trials

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.

Other records listing Lunar Corp. as applicant

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.

View all 23 devices →

Related Devices (Code: KGI)

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.

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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