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FDA 510(k)

SPIRTIUS CUFF INFLATION SYRINGE

K-Number: K112915 · 2012-05-25

ApplicantSpiritus Technologies, LLC
Decision Date2012-05-25
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPIRTIUS CUFF INFLATION SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Spiritus Technologies, LLC. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K112915. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIRTIUS CUFF INFLATION SYRINGE?

SPIRTIUS CUFF INFLATION SYRINGE is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Spiritus Technologies, LLC. The 510(k) number is K112915.

When did SPIRTIUS CUFF INFLATION SYRINGE receive FDA 510(k) clearance?

SPIRTIUS CUFF INFLATION SYRINGE received FDA 510(k) clearance on 2012-05-25, under 510(k) number K112915.

Who is the listed applicant for SPIRTIUS CUFF INFLATION SYRINGE?

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

What is the FDA product code for SPIRTIUS CUFF INFLATION SYRINGE?

The FDA product code for SPIRTIUS CUFF INFLATION SYRINGE is BSK.

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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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