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FDA 510(k)

PSL BIOZIR BLOCK

K-Number: K073568 · 2008-02-06

ApplicantP.S.L. International, Inc.
Decision Date2008-02-06
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PSL BIOZIR BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is P.S.L. International, Inc.. It received FDA 510(k) clearance on 2008-02-06 under 510(k) number K073568. 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 PSL BIOZIR BLOCK?

PSL BIOZIR BLOCK is a medical device that received FDA 510(k) clearance on 2008-02-06. The listed applicant is P.S.L. International, Inc.. The 510(k) number is K073568.

When did PSL BIOZIR BLOCK receive FDA 510(k) clearance?

PSL BIOZIR BLOCK received FDA 510(k) clearance on 2008-02-06, under 510(k) number K073568.

Who is the listed applicant for PSL BIOZIR BLOCK?

The FDA 510(k) record lists P.S.L. International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PSL BIOZIR BLOCK?

The FDA product code for PSL BIOZIR BLOCK 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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