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FDA 510(k)

WURTZ CHOLEY CLIP (TM)

K-Number: K901520 · 1990-06-26

Decision Date1990-06-26
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WURTZ CHOLEY CLIP (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Cd Medical, Inc.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K901520. 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 WURTZ CHOLEY CLIP (TM)?

WURTZ CHOLEY CLIP (TM) is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is Cd Medical, Inc.. The 510(k) number is K901520.

When did WURTZ CHOLEY CLIP (TM) receive FDA 510(k) clearance?

WURTZ CHOLEY CLIP (TM) received FDA 510(k) clearance on 1990-06-26, under 510(k) number K901520.

Who is the listed applicant for WURTZ CHOLEY CLIP (TM)?

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

What is the FDA product code for WURTZ CHOLEY CLIP (TM)?

The FDA product code for WURTZ CHOLEY CLIP (TM) 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 Cd Medical, 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 11 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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