STAR SYNC, MODIFICATION
K-Number: K913972 · 1992-01-09
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Device Summary
Frequently Asked Questions
What is the STAR SYNC, MODIFICATION?
STAR SYNC, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Infrasonics Corp.. The 510(k) number is K913972.
When did STAR SYNC, MODIFICATION receive FDA 510(k) clearance?
STAR SYNC, MODIFICATION received FDA 510(k) clearance on 1992-01-09, under 510(k) number K913972.
Who is the listed applicant for STAR SYNC, MODIFICATION?
The FDA 510(k) record lists Infrasonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STAR SYNC, MODIFICATION?
The FDA product code for STAR SYNC, MODIFICATION is CBK.
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 Infrasonics 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: CBK)
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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