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FDA 510(k)

BLOOD GAS EXPERSYSTEM 8700

K-Number: K833430 · 1984-02-10

ApplicantMedical Intelcom, Inc.
Decision Date1984-02-10
Product CodeLLE
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS EXPERSYSTEM 8700 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Intelcom, Inc.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K833430. The device is classified under product code LLE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS EXPERSYSTEM 8700?

BLOOD GAS EXPERSYSTEM 8700 is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Medical Intelcom, Inc.. The 510(k) number is K833430.

When did BLOOD GAS EXPERSYSTEM 8700 receive FDA 510(k) clearance?

BLOOD GAS EXPERSYSTEM 8700 received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833430.

Who is the listed applicant for BLOOD GAS EXPERSYSTEM 8700?

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

What is the FDA product code for BLOOD GAS EXPERSYSTEM 8700?

The FDA product code for BLOOD GAS EXPERSYSTEM 8700 is LLE.

Related Clinical Trials

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Related Devices (Code: LLE)

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.

K832916INIVOX ELECTRODE/CATHETER SYSCritikon Company, LLC

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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