FDA 510(k)

BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM

K-Number: K884063 · 1988-12-16

Decision Date1988-12-16

Product CodeCCE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1988-12-16 under 510(k) number K884063. The device is classified under product code CCE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM?

BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM is a medical device that received FDA 510(k) clearance on 1988-12-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K884063.

When did BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM receive FDA 510(k) clearance?

BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM received FDA 510(k) clearance on 1988-12-16, under 510(k) number K884063.

Who is the listed applicant for BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM?

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

What is the FDA product code for BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM?

The FDA product code for BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM is CCE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.