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FDA 510(k)

ATRAUMATIC VASCULAR CLAMPS

K-Number: K102048 · 2010-11-09

ApplicantGeomed Medizin-Technik GmbH & Co. KG
Decision Date2010-11-09
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATRAUMATIC VASCULAR CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2010-11-09 under 510(k) number K102048. 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 ATRAUMATIC VASCULAR CLAMPS?

ATRAUMATIC VASCULAR CLAMPS is a medical device that received FDA 510(k) clearance on 2010-11-09. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. The 510(k) number is K102048.

When did ATRAUMATIC VASCULAR CLAMPS receive FDA 510(k) clearance?

ATRAUMATIC VASCULAR CLAMPS received FDA 510(k) clearance on 2010-11-09, under 510(k) number K102048.

Who is the listed applicant for ATRAUMATIC VASCULAR CLAMPS?

The FDA 510(k) record lists Geomed Medizin-Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATRAUMATIC VASCULAR CLAMPS?

The FDA product code for ATRAUMATIC VASCULAR CLAMPS is DXC.

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Other records listing Geomed Medizin-Technik GmbH & Co. KG as applicant

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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.

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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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