RUSCH MEMORY BAG
K-Number: K013872 · 2002-02-12
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Device Summary
Frequently Asked Questions
What is the RUSCH MEMORY BAG?
RUSCH MEMORY BAG is a medical device that received FDA 510(k) clearance on 2002-02-12. The listed applicant is Rusch Intl.. The 510(k) number is K013872.
When did RUSCH MEMORY BAG receive FDA 510(k) clearance?
RUSCH MEMORY BAG received FDA 510(k) clearance on 2002-02-12, under 510(k) number K013872.
Who is the listed applicant for RUSCH MEMORY BAG?
The FDA 510(k) record lists Rusch Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUSCH MEMORY BAG?
The FDA product code for RUSCH MEMORY BAG is GCJ.
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 Rusch Intl. 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: GCJ)
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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