ANADIAS NASAL SAW BLADES
K-Number: K854192 · 1985-11-13
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Device Summary
Frequently Asked Questions
What is the ANADIAS NASAL SAW BLADES?
ANADIAS NASAL SAW BLADES is a medical device that received FDA 510(k) clearance on 1985-11-13. The listed applicant is Anadias, Inc.. The 510(k) number is K854192.
When did ANADIAS NASAL SAW BLADES receive FDA 510(k) clearance?
ANADIAS NASAL SAW BLADES received FDA 510(k) clearance on 1985-11-13, under 510(k) number K854192.
Who is the listed applicant for ANADIAS NASAL SAW BLADES?
The FDA 510(k) record lists Anadias, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANADIAS NASAL SAW BLADES?
The FDA product code for ANADIAS NASAL SAW BLADES 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 Anadias, 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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