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FDA 510(k)

ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE

K-Number: K901565 · 1990-06-12

Decision Date1990-06-12
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE is the device name listed in this FDA 510(k) record. The listed applicant is Applied Vascular Devices, Inc.. It received FDA 510(k) clearance on 1990-06-12 under 510(k) number K901565. 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 MODEL FOG-5048, 75MM SIDE?

ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE is a medical device that received FDA 510(k) clearance on 1990-06-12. The listed applicant is Applied Vascular Devices, Inc.. The 510(k) number is K901565.

When did ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE receive FDA 510(k) clearance?

ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE received FDA 510(k) clearance on 1990-06-12, under 510(k) number K901565.

Who is the listed applicant for ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE?

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

What is the FDA product code for ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE?

The FDA product code for ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE 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 Vascular Devices, 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 21 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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