MICRO-AIRE REPLACEMENT SURG. SAW BLADE
K-Number: K831714 · 1983-07-07
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Device Summary
Frequently Asked Questions
What is the MICRO-AIRE REPLACEMENT SURG. SAW BLADE?
MICRO-AIRE REPLACEMENT SURG. SAW BLADE is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K831714.
When did MICRO-AIRE REPLACEMENT SURG. SAW BLADE receive FDA 510(k) clearance?
MICRO-AIRE REPLACEMENT SURG. SAW BLADE received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831714.
Who is the listed applicant for MICRO-AIRE REPLACEMENT SURG. SAW BLADE?
The FDA 510(k) record lists Micro-Aire Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-AIRE REPLACEMENT SURG. SAW BLADE?
The FDA product code for MICRO-AIRE REPLACEMENT SURG. SAW BLADE is GFA.
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-Aire Surgical Instruments, 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: GFA)
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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