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FDA 510(k)

Z-BLOCK, MODELS 20/19, 40/19, 55/19

K-Number: K062389 · 2006-08-21

ApplicantFoundation Milling Centre
Decision Date2006-08-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Z-BLOCK, MODELS 20/19, 40/19, 55/19 is the device name listed in this FDA 510(k) record. The listed applicant is Foundation Milling Centre. It received FDA 510(k) clearance on 2006-08-21 under 510(k) number K062389. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z-BLOCK, MODELS 20/19, 40/19, 55/19?

Z-BLOCK, MODELS 20/19, 40/19, 55/19 is a medical device that received FDA 510(k) clearance on 2006-08-21. The listed applicant is Foundation Milling Centre. The 510(k) number is K062389.

When did Z-BLOCK, MODELS 20/19, 40/19, 55/19 receive FDA 510(k) clearance?

Z-BLOCK, MODELS 20/19, 40/19, 55/19 received FDA 510(k) clearance on 2006-08-21, under 510(k) number K062389.

Who is the listed applicant for Z-BLOCK, MODELS 20/19, 40/19, 55/19?

The FDA 510(k) record lists Foundation Milling Centre as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Z-BLOCK, MODELS 20/19, 40/19, 55/19?

The FDA product code for Z-BLOCK, MODELS 20/19, 40/19, 55/19 is EIH.

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Related Devices (Code: EIH)

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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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