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FDA 510(k)

ARTERIAL BLOOD GAS INTERPRETATION PROG

K-Number: K840102 · 1984-02-04

ApplicantM. D. Software, Inc.
Decision Date1984-02-04
Product CodeCCE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARTERIAL BLOOD GAS INTERPRETATION PROG is the device name listed in this FDA 510(k) record. The listed applicant is M. D. Software, Inc.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K840102. 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 ARTERIAL BLOOD GAS INTERPRETATION PROG?

ARTERIAL BLOOD GAS INTERPRETATION PROG is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is M. D. Software, Inc.. The 510(k) number is K840102.

When did ARTERIAL BLOOD GAS INTERPRETATION PROG receive FDA 510(k) clearance?

ARTERIAL BLOOD GAS INTERPRETATION PROG received FDA 510(k) clearance on 1984-02-04, under 510(k) number K840102.

Who is the listed applicant for ARTERIAL BLOOD GAS INTERPRETATION PROG?

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

What is the FDA product code for ARTERIAL BLOOD GAS INTERPRETATION PROG?

The FDA product code for ARTERIAL BLOOD GAS INTERPRETATION PROG is CCE.

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Related Devices (Code: CCE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K935778VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEMVia Medical Corp.K912145SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIAS & W Medico TeknikK910453TOPS NEEDLE TIP PROBE & PVC TIP PROBEBaxter Healthcare CorpK905397PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEMPuritan Bennett Corp.K896311OPTEX BLOOD GAS MONITORING SYSTEMOptex BiomedicalK890624TISSUE OXYGEN MONITOR SYSTEM, MODEL IIBaxter Healthcare Corp

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.

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