MICROFLATOR
K-Number: K771679 · 1977-09-28
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Device Summary
Frequently Asked Questions
What is the MICROFLATOR?
MICROFLATOR is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Fisons Corp.. The 510(k) number is K771679.
When did MICROFLATOR receive FDA 510(k) clearance?
MICROFLATOR received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771679.
Who is the listed applicant for MICROFLATOR?
The FDA 510(k) record lists Fisons Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROFLATOR?
The FDA product code for MICROFLATOR is FLG.
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 Fisons 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: FLG)
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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