MICRO BLADE II
K-Number: K812526 · 1981-09-16
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Device Summary
Frequently Asked Questions
What is the MICRO BLADE II?
MICRO BLADE II is a medical device that received FDA 510(k) clearance on 1981-09-16. The listed applicant is Vxtra Corp.. The 510(k) number is K812526.
When did MICRO BLADE II receive FDA 510(k) clearance?
MICRO BLADE II received FDA 510(k) clearance on 1981-09-16, under 510(k) number K812526.
Who is the listed applicant for MICRO BLADE II?
The FDA 510(k) record lists Vxtra Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO BLADE II?
The FDA product code for MICRO BLADE II is GES.
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 Vxtra Corp. 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: GES)
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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