STRYKER SWITCHPOINT INFINITY
K-Number: K033132 · 2004-09-02
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Device Summary
Frequently Asked Questions
What is the STRYKER SWITCHPOINT INFINITY?
STRYKER SWITCHPOINT INFINITY is a medical device that received FDA 510(k) clearance on 2004-09-02. The listed applicant is Stryker Communications Corp.. The 510(k) number is K033132.
When did STRYKER SWITCHPOINT INFINITY receive FDA 510(k) clearance?
STRYKER SWITCHPOINT INFINITY received FDA 510(k) clearance on 2004-09-02, under 510(k) number K033132.
Who is the listed applicant for STRYKER SWITCHPOINT INFINITY?
The FDA 510(k) record lists Stryker Communications Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER SWITCHPOINT INFINITY?
The FDA product code for STRYKER SWITCHPOINT INFINITY 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 Stryker Communications Corp. 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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