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FDA 510(k)

COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION

K-Number: K871490 · 1987-12-07

ApplicantGe Medical Systems Information Technologies
Decision Date1987-12-07
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1987-12-07 under 510(k) number K871490. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION?

COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K871490.

When did COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION receive FDA 510(k) clearance?

COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION received FDA 510(k) clearance on 1987-12-07, under 510(k) number K871490.

Who is the listed applicant for COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION?

The FDA product code for COLORVIEW 860 OR SSD-860 PULSE ECHO/MODIFICATION is DPW.

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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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