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FDA 510(k)

MEDITECH EUROSCANNER M250

K-Number: K850027 · 1985-04-04

ApplicantStuart Medical, Inc.
Decision Date1985-04-04
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDITECH EUROSCANNER M250 is the device name listed in this FDA 510(k) record. The listed applicant is Stuart Medical, Inc.. It received FDA 510(k) clearance on 1985-04-04 under 510(k) number K850027. 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 MEDITECH EUROSCANNER M250?

MEDITECH EUROSCANNER M250 is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Stuart Medical, Inc.. The 510(k) number is K850027.

When did MEDITECH EUROSCANNER M250 receive FDA 510(k) clearance?

MEDITECH EUROSCANNER M250 received FDA 510(k) clearance on 1985-04-04, under 510(k) number K850027.

Who is the listed applicant for MEDITECH EUROSCANNER M250?

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

What is the FDA product code for MEDITECH EUROSCANNER M250?

The FDA product code for MEDITECH EUROSCANNER M250 is JAK.

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Other records listing Stuart Medical, Inc. as applicant

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Related Devices (Code: JAK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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