DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)
K-Number: K983129 · 1998-12-04
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)?
DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) is a medical device that received FDA 510(k) clearance on 1998-12-04. The listed applicant is Staar Surgical Co.. The 510(k) number is K983129.
When did DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) receive FDA 510(k) clearance?
DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) received FDA 510(k) clearance on 1998-12-04, under 510(k) number K983129.
Who is the listed applicant for DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)?
The FDA 510(k) record lists Staar Surgical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)?
The FDA product code for DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) is KYB.
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 Staar Surgical Co. 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: KYB)
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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