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FDA 510(k)

ZIRBLOCK

K-Number: K070537 · 2007-04-30

ApplicantCdl Technologies, Inc.
Decision Date2007-04-30
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZIRBLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Cdl Technologies, Inc.. It received FDA 510(k) clearance on 2007-04-30 under 510(k) number K070537. 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 ZIRBLOCK?

ZIRBLOCK is a medical device that received FDA 510(k) clearance on 2007-04-30. The listed applicant is Cdl Technologies, Inc.. The 510(k) number is K070537.

When did ZIRBLOCK receive FDA 510(k) clearance?

ZIRBLOCK received FDA 510(k) clearance on 2007-04-30, under 510(k) number K070537.

Who is the listed applicant for ZIRBLOCK?

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

What is the FDA product code for ZIRBLOCK?

The FDA product code for ZIRBLOCK 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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