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FDA 510(k)

ATRAUMAX SURGICAL CLAMP

K-Number: K950492 · 1995-05-08

Decision Date1995-05-08
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATRAUMAX SURGICAL CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1995-05-08 under 510(k) number K950492. 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 ATRAUMAX SURGICAL CLAMP?

ATRAUMAX SURGICAL CLAMP is a medical device that received FDA 510(k) clearance on 1995-05-08. The listed applicant is Applied Medical Resources. The 510(k) number is K950492.

When did ATRAUMAX SURGICAL CLAMP receive FDA 510(k) clearance?

ATRAUMAX SURGICAL CLAMP received FDA 510(k) clearance on 1995-05-08, under 510(k) number K950492.

Who is the listed applicant for ATRAUMAX SURGICAL CLAMP?

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

What is the FDA product code for ATRAUMAX SURGICAL CLAMP?

The FDA product code for ATRAUMAX SURGICAL 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 Applied Medical Resources 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 53 devices →

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

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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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