COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT
K-Number: K992906 · 1999-11-10
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Device Summary
Frequently Asked Questions
What is the COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT?
COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Olson Medical Sales, Inc.. The 510(k) number is K992906.
When did COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT receive FDA 510(k) clearance?
COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT received FDA 510(k) clearance on 1999-11-10, under 510(k) number K992906.
Who is the listed applicant for COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT?
The FDA 510(k) record lists Olson Medical Sales, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT?
The FDA product code for COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT is DTL.
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 Olson Medical Sales, 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: DTL)
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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