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FDA 510(k)

THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP

K-Number: K993424 · 1999-12-23

ApplicantY-Clip Associates
Decision Date1999-12-23
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Y-Clip Associates. It received FDA 510(k) clearance on 1999-12-23 under 510(k) number K993424. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP?

THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP is a medical device that received FDA 510(k) clearance on 1999-12-23. The listed applicant is Y-Clip Associates. The 510(k) number is K993424.

When did THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP receive FDA 510(k) clearance?

THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP received FDA 510(k) clearance on 1999-12-23, under 510(k) number K993424.

Who is the listed applicant for THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP?

The FDA 510(k) record lists Y-Clip Associates as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP?

The FDA product code for THE TRUE Y CLIP, THE MICRO Y CLIP, THE LAPAROSCOPIC Y CLIP is FZP.

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Related Devices (Code: FZP)

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

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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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