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FDA 510(k)

SELF-LATCHING CLIP

K-Number: K945231 · 1995-01-27

Decision Date1995-01-27
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SELF-LATCHING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Surgical System, Inc.. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K945231. 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 SELF-LATCHING CLIP?

SELF-LATCHING CLIP is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Surgical System, Inc.. The 510(k) number is K945231.

When did SELF-LATCHING CLIP receive FDA 510(k) clearance?

SELF-LATCHING CLIP received FDA 510(k) clearance on 1995-01-27, under 510(k) number K945231.

Who is the listed applicant for SELF-LATCHING CLIP?

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

What is the FDA product code for SELF-LATCHING CLIP?

The FDA product code for SELF-LATCHING CLIP is FZP.

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: 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.

Official Source

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