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FDA 510(k)

MCKESSON ANESTHESIA CARE

K-Number: K113633 · 2012-04-20

ApplicantMckesson Technologies, Inc.
Decision Date2012-04-20
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MCKESSON ANESTHESIA CARE is the device name listed in this FDA 510(k) record. The listed applicant is Mckesson Technologies, Inc.. It received FDA 510(k) clearance on 2012-04-20 under 510(k) number K113633. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCKESSON ANESTHESIA CARE?

MCKESSON ANESTHESIA CARE is a medical device that received FDA 510(k) clearance on 2012-04-20. The listed applicant is Mckesson Technologies, Inc.. The 510(k) number is K113633.

When did MCKESSON ANESTHESIA CARE receive FDA 510(k) clearance?

MCKESSON ANESTHESIA CARE received FDA 510(k) clearance on 2012-04-20, under 510(k) number K113633.

Who is the listed applicant for MCKESSON ANESTHESIA CARE?

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

What is the FDA product code for MCKESSON ANESTHESIA CARE?

The FDA product code for MCKESSON ANESTHESIA CARE is BSZ.

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Related Devices (Code: BSZ)

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Official Source

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