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FDA 510(k)

LMI CHOLANGIOGRAM TRAY

K-Number: K873471 · 1987-10-23

Decision Date1987-10-23
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LMI CHOLANGIOGRAM TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Lazarus Medical Innovations, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K873471. The device is classified under product code GBZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMI CHOLANGIOGRAM TRAY?

LMI CHOLANGIOGRAM TRAY is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Lazarus Medical Innovations, Inc.. The 510(k) number is K873471.

When did LMI CHOLANGIOGRAM TRAY receive FDA 510(k) clearance?

LMI CHOLANGIOGRAM TRAY received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873471.

Who is the listed applicant for LMI CHOLANGIOGRAM TRAY?

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

What is the FDA product code for LMI CHOLANGIOGRAM TRAY?

The FDA product code for LMI CHOLANGIOGRAM TRAY is GBZ.

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.

Related Devices (Code: GBZ)

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

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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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