Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

S&T SINGLE USE MICRO ANASTOMOSIS CLAMP

K-Number: K022754 · 2002-10-16

ApplicantS & T AG
Decision Date2002-10-16
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

S&T SINGLE USE MICRO ANASTOMOSIS CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is S & T AG. It received FDA 510(k) clearance on 2002-10-16 under 510(k) number K022754. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S&T SINGLE USE MICRO ANASTOMOSIS CLAMP?

S&T SINGLE USE MICRO ANASTOMOSIS CLAMP is a medical device that received FDA 510(k) clearance on 2002-10-16. The listed applicant is S & T AG. The 510(k) number is K022754.

When did S&T SINGLE USE MICRO ANASTOMOSIS CLAMP receive FDA 510(k) clearance?

S&T SINGLE USE MICRO ANASTOMOSIS CLAMP received FDA 510(k) clearance on 2002-10-16, under 510(k) number K022754.

Who is the listed applicant for S&T SINGLE USE MICRO ANASTOMOSIS CLAMP?

The FDA 510(k) record lists S & T AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S&T SINGLE USE MICRO ANASTOMOSIS CLAMP?

The FDA product code for S&T SINGLE USE MICRO ANASTOMOSIS CLAMP is DXC.

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 S & T AG 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.

Related Devices (Code: DXC)

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.

↑