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FDA 510(k)

MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200

K-Number: K082565 · 2009-02-12

Decision Date2009-02-12
Product CodeNEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200 is the device name listed in this FDA 510(k) record. The listed applicant is Microsurgeon, Inc.. It received FDA 510(k) clearance on 2009-02-12 under 510(k) number K082565. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200?

MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200 is a medical device that received FDA 510(k) clearance on 2009-02-12. The listed applicant is Microsurgeon, Inc.. The 510(k) number is K082565.

When did MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200 receive FDA 510(k) clearance?

MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200 received FDA 510(k) clearance on 2009-02-12, under 510(k) number K082565.

Who is the listed applicant for MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200?

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

What is the FDA product code for MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200?

The FDA product code for MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-200 is NEY.

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 Microsurgeon, 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.

Related Devices (Code: NEY)

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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