MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100
K-Number: K070023 · 2007-08-15
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Device Summary
Frequently Asked Questions
What is the MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100?
MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100 is a medical device that received FDA 510(k) clearance on 2007-08-15. The listed applicant is Microsurgeon, Inc.. The 510(k) number is K070023.
When did MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100 receive FDA 510(k) clearance?
MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100 received FDA 510(k) clearance on 2007-08-15, under 510(k) number K070023.
Who is the listed applicant for MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100?
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-100?
The FDA product code for MICROSURGEON MICROWAVE TISSUE ABLATION DEVICE, MODEL MTAD-100 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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