Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

QCT-BONE MINERAL ANALYSIS SOFTWARE

K-Number: K941127 · 1995-05-11

Decision Date1995-05-11
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QCT-BONE MINERAL ANALYSIS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Image Analysis, Inc.. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K941127. 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 QCT-BONE MINERAL ANALYSIS SOFTWARE?

QCT-BONE MINERAL ANALYSIS SOFTWARE is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is Image Analysis, Inc.. The 510(k) number is K941127.

When did QCT-BONE MINERAL ANALYSIS SOFTWARE receive FDA 510(k) clearance?

QCT-BONE MINERAL ANALYSIS SOFTWARE received FDA 510(k) clearance on 1995-05-11, under 510(k) number K941127.

Who is the listed applicant for QCT-BONE MINERAL ANALYSIS SOFTWARE?

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

What is the FDA product code for QCT-BONE MINERAL ANALYSIS SOFTWARE?

The FDA product code for QCT-BONE MINERAL ANALYSIS SOFTWARE 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 Image Analysis, Inc. 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 9 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.

↑