AUTOGENESIS AUTOMATOR, MODEL M1000
K-Number: K013818 · 2001-12-05
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Device Summary
Frequently Asked Questions
What is the AUTOGENESIS AUTOMATOR, MODEL M1000?
AUTOGENESIS AUTOMATOR, MODEL M1000 is a medical device that received FDA 510(k) clearance on 2001-12-05. The listed applicant is Autogenesis, Inc.. The 510(k) number is K013818.
When did AUTOGENESIS AUTOMATOR, MODEL M1000 receive FDA 510(k) clearance?
AUTOGENESIS AUTOMATOR, MODEL M1000 received FDA 510(k) clearance on 2001-12-05, under 510(k) number K013818.
Who is the listed applicant for AUTOGENESIS AUTOMATOR, MODEL M1000?
The FDA 510(k) record lists Autogenesis, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOGENESIS AUTOMATOR, MODEL M1000?
The FDA product code for AUTOGENESIS AUTOMATOR, MODEL M1000 is JEC.
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 Autogenesis, 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: JEC)
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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