DISPOSABLE ARACHNOID KNIFE
K-Number: K882422 · 1988-09-06
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE ARACHNOID KNIFE?
DISPOSABLE ARACHNOID KNIFE is a medical device that received FDA 510(k) clearance on 1988-09-06. The listed applicant is Microbio-Medics, Inc.. The 510(k) number is K882422.
When did DISPOSABLE ARACHNOID KNIFE receive FDA 510(k) clearance?
DISPOSABLE ARACHNOID KNIFE received FDA 510(k) clearance on 1988-09-06, under 510(k) number K882422.
Who is the listed applicant for DISPOSABLE ARACHNOID KNIFE?
The FDA 510(k) record lists Microbio-Medics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE ARACHNOID KNIFE?
The FDA product code for DISPOSABLE ARACHNOID KNIFE is HAO.
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 Microbio-Medics, 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: HAO)
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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