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FDA 510(k)

HICOR

K-Number: K903375 · 1990-10-01

ApplicantSiemens Gammasonics, Inc.
Decision Date1990-10-01
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HICOR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1990-10-01 under 510(k) number K903375. 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 HICOR?

HICOR is a medical device that received FDA 510(k) clearance on 1990-10-01. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K903375.

When did HICOR receive FDA 510(k) clearance?

HICOR received FDA 510(k) clearance on 1990-10-01, under 510(k) number K903375.

Who is the listed applicant for HICOR?

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

What is the FDA product code for HICOR?

The FDA product code for HICOR is IZI.

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Other records listing Siemens Gammasonics, Inc. as applicant

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Related Devices (Code: 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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