RAVEN PROPACT
K-Number: K053212 · 2006-02-15
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Device Summary
Frequently Asked Questions
What is the RAVEN PROPACT?
RAVEN PROPACT is a medical device that received FDA 510(k) clearance on 2006-02-15. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K053212.
When did RAVEN PROPACT receive FDA 510(k) clearance?
RAVEN PROPACT received FDA 510(k) clearance on 2006-02-15, under 510(k) number K053212.
Who is the listed applicant for RAVEN PROPACT?
The FDA 510(k) record lists Raven Biological Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAVEN PROPACT?
The FDA product code for RAVEN PROPACT is MRB.
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 Raven Biological Laboratories, 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: MRB)
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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