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FDA 510(k)

MORTARA STRESS ECHO BED

K-Number: K082967 · 2009-03-26

ApplicantMedical Positioning, Inc.
Decision Date2009-03-26
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA STRESS ECHO BED is the device name listed in this FDA 510(k) record. The listed applicant is Medical Positioning, Inc.. It received FDA 510(k) clearance on 2009-03-26 under 510(k) number K082967. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORTARA STRESS ECHO BED?

MORTARA STRESS ECHO BED is a medical device that received FDA 510(k) clearance on 2009-03-26. The listed applicant is Medical Positioning, Inc.. The 510(k) number is K082967.

When did MORTARA STRESS ECHO BED receive FDA 510(k) clearance?

MORTARA STRESS ECHO BED received FDA 510(k) clearance on 2009-03-26, under 510(k) number K082967.

Who is the listed applicant for MORTARA STRESS ECHO BED?

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

What is the FDA product code for MORTARA STRESS ECHO BED?

The FDA product code for MORTARA STRESS ECHO BED is DPS.

Related Clinical Trials

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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Other records listing Medical Positioning, Inc. as applicant

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.

K021171Q-STRESS ECHO BEDK002822VERTEX SYSTEM

Related Devices (Code: DPS)

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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