FDA 510(k)

PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS

K-Number: K863033 · 1986-08-20

Decision Date1986-08-20

Product CodeBZO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS is the device name listed in this FDA 510(k) record. The listed applicant is Intertech/Ohio. It received FDA 510(k) clearance on 1986-08-20 under 510(k) number K863033. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS?

PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS is a medical device that received FDA 510(k) clearance on 1986-08-20. The listed applicant is Intertech/Ohio. The 510(k) number is K863033.

When did PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS receive FDA 510(k) clearance?

PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS received FDA 510(k) clearance on 1986-08-20, under 510(k) number K863033.

Who is the listed applicant for PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS?

The FDA 510(k) record lists Intertech/Ohio as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS?

The FDA product code for PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS is BZO.

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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.