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FDA 510(k)

EPCOR

K-Number: K930786 · 1994-09-26

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-09-26
Product CodeDRW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EPCOR 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 1994-09-26 under 510(k) number K930786. The device is classified under product code DRW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPCOR?

EPCOR is a medical device that received FDA 510(k) clearance on 1994-09-26. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K930786.

When did EPCOR receive FDA 510(k) clearance?

EPCOR received FDA 510(k) clearance on 1994-09-26, under 510(k) number K930786.

Who is the listed applicant for EPCOR?

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 EPCOR?

The FDA product code for EPCOR is DRW.

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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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