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FDA 510(k)

ANCOR

K-Number: K924719 · 1992-12-30

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1992-12-30
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANCOR 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 1992-12-30 under 510(k) number K924719. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANCOR?

ANCOR is a medical device that received FDA 510(k) clearance on 1992-12-30. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K924719.

When did ANCOR receive FDA 510(k) clearance?

ANCOR received FDA 510(k) clearance on 1992-12-30, under 510(k) number K924719.

Who is the listed applicant for ANCOR?

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 ANCOR?

The FDA product code for ANCOR is IZI.

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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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