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FDA 510(k)

CAREGRAPH

K-Number: K982319 · 1998-09-22

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1998-09-22
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAREGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1998-09-22 under 510(k) number K982319. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAREGRAPH?

CAREGRAPH is a medical device that received FDA 510(k) clearance on 1998-09-22. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K982319.

When did CAREGRAPH receive FDA 510(k) clearance?

CAREGRAPH received FDA 510(k) clearance on 1998-09-22, under 510(k) number K982319.

Who is the listed applicant for CAREGRAPH?

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

What is the FDA product code for CAREGRAPH?

The FDA product code for CAREGRAPH is JAA.

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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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