FDA 510(k)

5543 INDEPENDENT VIEWING SYSTEM

K-Number: K780930 · 1978-06-14

Decision Date1978-06-14

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

5543 INDEPENDENT VIEWING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Emi Medical, Inc.. It received FDA 510(k) clearance on 1978-06-14 under 510(k) number K780930. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5543 INDEPENDENT VIEWING SYSTEM?

5543 INDEPENDENT VIEWING SYSTEM is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Emi Medical, Inc.. The 510(k) number is K780930.

When did 5543 INDEPENDENT VIEWING SYSTEM receive FDA 510(k) clearance?

5543 INDEPENDENT VIEWING SYSTEM received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780930.

Who is the listed applicant for 5543 INDEPENDENT VIEWING SYSTEM?

The FDA 510(k) record lists Emi Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 5543 INDEPENDENT VIEWING SYSTEM?

The FDA product code for 5543 INDEPENDENT VIEWING SYSTEM is JAK.

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Other records listing Emi Medical, Inc. as applicant

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Related Devices (Code: JAK)

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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.