MICRO-AIRE MODEL 2060
K-Number: K913369 · 1991-11-01
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Device Summary
Frequently Asked Questions
What is the MICRO-AIRE MODEL 2060?
MICRO-AIRE MODEL 2060 is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K913369.
When did MICRO-AIRE MODEL 2060 receive FDA 510(k) clearance?
MICRO-AIRE MODEL 2060 received FDA 510(k) clearance on 1991-11-01, under 510(k) number K913369.
Who is the listed applicant for MICRO-AIRE MODEL 2060?
The FDA 510(k) record lists Micro Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-AIRE MODEL 2060?
The FDA product code for MICRO-AIRE MODEL 2060 is GEY.
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 Micro Surgical Instruments 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: GEY)
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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