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FDA 510(k)

SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH

K-Number: K903709 · 1990-10-26

Decision Date1990-10-26
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH is the device name listed in this FDA 510(k) record. The listed applicant is Lifestream Int'L, Inc.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K903709. 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 SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH?

SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Lifestream Int'L, Inc.. The 510(k) number is K903709.

When did SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH receive FDA 510(k) clearance?

SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH received FDA 510(k) clearance on 1990-10-26, under 510(k) number K903709.

Who is the listed applicant for SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH?

The FDA 510(k) record lists Lifestream Int'L, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH?

The FDA product code for SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH 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.

Other records listing Lifestream Int'L, 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 23 devices →

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

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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