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FDA 510(k)

KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5

K-Number: K071195 · 2007-06-20

ApplicantAni-Kal Ii, LLC
Decision Date2007-06-20
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5 is the device name listed in this FDA 510(k) record. The listed applicant is Ani-Kal Ii, LLC. It received FDA 510(k) clearance on 2007-06-20 under 510(k) number K071195. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5?

KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5 is a medical device that received FDA 510(k) clearance on 2007-06-20. The listed applicant is Ani-Kal Ii, LLC. The 510(k) number is K071195.

When did KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5 receive FDA 510(k) clearance?

KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5 received FDA 510(k) clearance on 2007-06-20, under 510(k) number K071195.

Who is the listed applicant for KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5?

The FDA 510(k) record lists Ani-Kal Ii, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5?

The FDA product code for KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5 is IYX.

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Related Devices (Code: IYX)

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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