SYMBIOS DISPOSABLE INFUSION PUMP KIT
K-Number: K051474 · 2005-07-01
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Device Summary
Frequently Asked Questions
What is the SYMBIOS DISPOSABLE INFUSION PUMP KIT?
SYMBIOS DISPOSABLE INFUSION PUMP KIT is a medical device that received FDA 510(k) clearance on 2005-07-01. The listed applicant is Symbios Medical Products, LLC. The 510(k) number is K051474.
When did SYMBIOS DISPOSABLE INFUSION PUMP KIT receive FDA 510(k) clearance?
SYMBIOS DISPOSABLE INFUSION PUMP KIT received FDA 510(k) clearance on 2005-07-01, under 510(k) number K051474.
Who is the listed applicant for SYMBIOS DISPOSABLE INFUSION PUMP KIT?
The FDA 510(k) record lists Symbios Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYMBIOS DISPOSABLE INFUSION PUMP KIT?
The FDA product code for SYMBIOS DISPOSABLE INFUSION PUMP KIT is MEB.
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 Symbios Medical Products, LLC 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: MEB)
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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