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FDA 510(k)

KEYFILL

K-Number: K872053 · 1987-07-01

ApplicantMayfield Instruments, Ltd.
Decision Date1987-07-01
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KEYFILL is the device name listed in this FDA 510(k) record. The listed applicant is Mayfield Instruments, Ltd.. It received FDA 510(k) clearance on 1987-07-01 under 510(k) number K872053. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEYFILL?

KEYFILL is a medical device that received FDA 510(k) clearance on 1987-07-01. The listed applicant is Mayfield Instruments, Ltd.. The 510(k) number is K872053.

When did KEYFILL receive FDA 510(k) clearance?

KEYFILL received FDA 510(k) clearance on 1987-07-01, under 510(k) number K872053.

Who is the listed applicant for KEYFILL?

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

What is the FDA product code for KEYFILL?

The FDA product code for KEYFILL is CAD.

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Related Devices (Code: CAD)

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.

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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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