ASTOFLO
K-Number: K020060 · 2002-03-05
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Device Summary
Frequently Asked Questions
What is the ASTOFLO?
ASTOFLO is a medical device that received FDA 510(k) clearance on 2002-03-05. The listed applicant is Nats Corp.. The 510(k) number is K020060.
When did ASTOFLO receive FDA 510(k) clearance?
ASTOFLO received FDA 510(k) clearance on 2002-03-05, under 510(k) number K020060.
Who is the listed applicant for ASTOFLO?
The FDA 510(k) record lists Nats Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASTOFLO?
The FDA product code for ASTOFLO is BSB.
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 Nats 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: BSB)
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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