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FDA 510(k)

TREND PROCESSOR OPTION FOR #515 NEONAT

K-Number: K833552 · 1984-01-27

ApplicantGe Medical Systems Information Technologies
Decision Date1984-01-27
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TREND PROCESSOR OPTION FOR #515 NEONAT 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 1984-01-27 under 510(k) number K833552. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREND PROCESSOR OPTION FOR #515 NEONAT?

TREND PROCESSOR OPTION FOR #515 NEONAT is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K833552.

When did TREND PROCESSOR OPTION FOR #515 NEONAT receive FDA 510(k) clearance?

TREND PROCESSOR OPTION FOR #515 NEONAT received FDA 510(k) clearance on 1984-01-27, under 510(k) number K833552.

Who is the listed applicant for TREND PROCESSOR OPTION FOR #515 NEONAT?

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 TREND PROCESSOR OPTION FOR #515 NEONAT?

The FDA product code for TREND PROCESSOR OPTION FOR #515 NEONAT is DRT.

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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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