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FDA 510(k)

I/A KIT

K-Number: K831159 · 1983-04-28

ApplicantStaar Surgical Co.
Decision Date1983-04-28
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

I/A KIT is the device name listed in this FDA 510(k) record. The listed applicant is Staar Surgical Co.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831159. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I/A KIT?

I/A KIT is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Staar Surgical Co.. The 510(k) number is K831159.

When did I/A KIT receive FDA 510(k) clearance?

I/A KIT received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831159.

Who is the listed applicant for I/A KIT?

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 I/A KIT?

The FDA product code for I/A KIT is JSM.

Other records listing Staar Surgical Co. as applicant

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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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