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FDA 510(k)

SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.

K-Number: K880217 · 1988-04-25

ApplicantGe Medical Systems Information Technologies
Decision Date1988-04-25
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN. 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 1988-04-25 under 510(k) number K880217. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.?

SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN. is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K880217.

When did SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN. receive FDA 510(k) clearance?

SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN. received FDA 510(k) clearance on 1988-04-25, under 510(k) number K880217.

Who is the listed applicant for SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.?

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 SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.?

The FDA product code for SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN. is DXK.

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Related Devices (Code: DXK)

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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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