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FDA 510(k)

GIOTTO MAMMOGRAPHY HF

K-Number: K901558 · 1990-07-03

ApplicantMedical Device Marketing Network, Inc.
Decision Date1990-07-03
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GIOTTO MAMMOGRAPHY HF is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Marketing Network, Inc.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K901558. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIOTTO MAMMOGRAPHY HF?

GIOTTO MAMMOGRAPHY HF is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Medical Device Marketing Network, Inc.. The 510(k) number is K901558.

When did GIOTTO MAMMOGRAPHY HF receive FDA 510(k) clearance?

GIOTTO MAMMOGRAPHY HF received FDA 510(k) clearance on 1990-07-03, under 510(k) number K901558.

Who is the listed applicant for GIOTTO MAMMOGRAPHY HF?

The FDA 510(k) record lists Medical Device Marketing Network, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GIOTTO MAMMOGRAPHY HF?

The FDA product code for GIOTTO MAMMOGRAPHY HF is IZH.

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Related Devices (Code: IZH)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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