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FDA 510(k)

CARDIAC WALL MOTION DEVICE

K-Number: K833728 · 1984-02-10

ApplicantIntl. Medical, Inc.
Decision Date1984-02-10
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIAC WALL MOTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical, Inc.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K833728. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIAC WALL MOTION DEVICE?

CARDIAC WALL MOTION DEVICE is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Intl. Medical, Inc.. The 510(k) number is K833728.

When did CARDIAC WALL MOTION DEVICE receive FDA 510(k) clearance?

CARDIAC WALL MOTION DEVICE received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833728.

Who is the listed applicant for CARDIAC WALL MOTION DEVICE?

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

What is the FDA product code for CARDIAC WALL MOTION DEVICE?

The FDA product code for CARDIAC WALL MOTION DEVICE is DSB.

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Other records listing Intl. Medical, Inc. as applicant

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Related Devices (Code: DSB)

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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.

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