FDA 510(k)

SCANNER-EMI 7020 AND 7020R

K-Number: K781936 · 1978-12-04

Decision Date1978-12-04

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SCANNER-EMI 7020 AND 7020R 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 1978-12-04 under 510(k) number K781936. 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 SCANNER-EMI 7020 AND 7020R?

SCANNER-EMI 7020 AND 7020R is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Emi Medical, Inc.. The 510(k) number is K781936.

When did SCANNER-EMI 7020 AND 7020R receive FDA 510(k) clearance?

SCANNER-EMI 7020 AND 7020R received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781936.

Who is the listed applicant for SCANNER-EMI 7020 AND 7020R?

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 SCANNER-EMI 7020 AND 7020R?

The FDA product code for SCANNER-EMI 7020 AND 7020R 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

View on FDA Database →

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