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FDA 510(k)

MODIFIED MODEL SSD-650 SYSTEM

K-Number: K873452 · 1988-07-28

ApplicantGe Medical Systems Information Technologies
Decision Date1988-07-28
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODEL SSD-650 SYSTEM 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 1988-07-28 under 510(k) number K873452. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MODEL SSD-650 SYSTEM?

MODIFIED MODEL SSD-650 SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K873452.

When did MODIFIED MODEL SSD-650 SYSTEM receive FDA 510(k) clearance?

MODIFIED MODEL SSD-650 SYSTEM received FDA 510(k) clearance on 1988-07-28, under 510(k) number K873452.

Who is the listed applicant for MODIFIED MODEL SSD-650 SYSTEM?

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 MODIFIED MODEL SSD-650 SYSTEM?

The FDA product code for MODIFIED MODEL SSD-650 SYSTEM is IYO.

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Other records listing Ge Medical Systems Information Technologies as applicant

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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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