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FDA 510(k)

MAMMOGRAPHY MOVING GRID BUCKY

K-Number: K880905 · 1988-03-21

Decision Date1988-03-21
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAMMOGRAPHY MOVING GRID BUCKY is the device name listed in this FDA 510(k) record. The listed applicant is Custom Medical Products, Ltd.. It received FDA 510(k) clearance on 1988-03-21 under 510(k) number K880905. 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 MAMMOGRAPHY MOVING GRID BUCKY?

MAMMOGRAPHY MOVING GRID BUCKY is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is Custom Medical Products, Ltd.. The 510(k) number is K880905.

When did MAMMOGRAPHY MOVING GRID BUCKY receive FDA 510(k) clearance?

MAMMOGRAPHY MOVING GRID BUCKY received FDA 510(k) clearance on 1988-03-21, under 510(k) number K880905.

Who is the listed applicant for MAMMOGRAPHY MOVING GRID BUCKY?

The FDA 510(k) record lists Custom Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAMMOGRAPHY MOVING GRID BUCKY?

The FDA product code for MAMMOGRAPHY MOVING GRID BUCKY is IZH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Custom Medical Products, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 13 devices →

Related Devices (Code: IZH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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