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FDA 510(k)

B-CAD SYSTEM, VERSION 1.0

K-Number: K050846 · 2005-05-26

ApplicantThe Medipattern Corporation
Decision Date2005-05-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

B-CAD SYSTEM, VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is The Medipattern Corporation. It received FDA 510(k) clearance on 2005-05-26 under 510(k) number K050846. 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 B-CAD SYSTEM, VERSION 1.0?

B-CAD SYSTEM, VERSION 1.0 is a medical device that received FDA 510(k) clearance on 2005-05-26. The listed applicant is The Medipattern Corporation. The 510(k) number is K050846.

When did B-CAD SYSTEM, VERSION 1.0 receive FDA 510(k) clearance?

B-CAD SYSTEM, VERSION 1.0 received FDA 510(k) clearance on 2005-05-26, under 510(k) number K050846.

Who is the listed applicant for B-CAD SYSTEM, VERSION 1.0?

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

What is the FDA product code for B-CAD SYSTEM, VERSION 1.0?

The FDA product code for B-CAD SYSTEM, VERSION 1.0 is LLZ.

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.

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Other records listing The Medipattern Corporation 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.

K103761VISUALIZE: VASCULAR

Related Devices (Code: LLZ)

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

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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