VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM
K-Number: K022225 · 2002-07-25
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Device Summary
Frequently Asked Questions
What is the VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM?
VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-25. The listed applicant is Vector Medical, Inc.. The 510(k) number is K022225.
When did VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM receive FDA 510(k) clearance?
VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM received FDA 510(k) clearance on 2002-07-25, under 510(k) number K022225.
Who is the listed applicant for VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM?
The FDA 510(k) record lists Vector Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM?
The FDA product code for VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM is HSB.
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 Vector Medical, 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: HSB)
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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