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FDA 510(k)

BLOOD GAS EXPER. SYSTEM 8700

K-Number: K822778 · 1982-12-03

ApplicantExper Corp., Inc.
Decision Date1982-12-03
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS EXPER. SYSTEM 8700 is the device name listed in this FDA 510(k) record. The listed applicant is Exper Corp., Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K822778. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS EXPER. SYSTEM 8700?

BLOOD GAS EXPER. SYSTEM 8700 is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Exper Corp., Inc.. The 510(k) number is K822778.

When did BLOOD GAS EXPER. SYSTEM 8700 receive FDA 510(k) clearance?

BLOOD GAS EXPER. SYSTEM 8700 received FDA 510(k) clearance on 1982-12-03, under 510(k) number K822778.

Who is the listed applicant for BLOOD GAS EXPER. SYSTEM 8700?

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

What is the FDA product code for BLOOD GAS EXPER. SYSTEM 8700?

The FDA product code for BLOOD GAS EXPER. SYSTEM 8700 is JQP.

Related Clinical Trials

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Related Devices (Code: JQP)

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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.

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