FDA 510(k)

TOMOGRAPHIC SCANNER, COMPUTERIZED

K-Number: K772125 · 1977-11-21

Decision Date1977-11-21

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

TOMOGRAPHIC SCANNER, COMPUTERIZED 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 1977-11-21 under 510(k) number K772125. 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 TOMOGRAPHIC SCANNER, COMPUTERIZED?

TOMOGRAPHIC SCANNER, COMPUTERIZED is a medical device that received FDA 510(k) clearance on 1977-11-21. The listed applicant is Emi Medical, Inc.. The 510(k) number is K772125.

When did TOMOGRAPHIC SCANNER, COMPUTERIZED receive FDA 510(k) clearance?

TOMOGRAPHIC SCANNER, COMPUTERIZED received FDA 510(k) clearance on 1977-11-21, under 510(k) number K772125.

Who is the listed applicant for TOMOGRAPHIC SCANNER, COMPUTERIZED?

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 TOMOGRAPHIC SCANNER, COMPUTERIZED?

The FDA product code for TOMOGRAPHIC SCANNER, COMPUTERIZED 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.