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FDA 510(k)

SYN-OPTICS #5200

K-Number: K820624 · 1982-04-01

ApplicantSyn-Optics
Decision Date1982-04-01
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYN-OPTICS #5200 is the device name listed in this FDA 510(k) record. The listed applicant is Syn-Optics. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820624. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYN-OPTICS #5200?

SYN-OPTICS #5200 is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Syn-Optics. The 510(k) number is K820624.

When did SYN-OPTICS #5200 receive FDA 510(k) clearance?

SYN-OPTICS #5200 received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820624.

Who is the listed applicant for SYN-OPTICS #5200?

The FDA 510(k) record lists Syn-Optics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYN-OPTICS #5200?

The FDA product code for SYN-OPTICS #5200 is FET.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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