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FDA 510(k)

AQUEOUS BLOOD GAS CONTROL

K-Number: K833146 · 1983-11-28

ApplicantBionostics, Inc.
Decision Date1983-11-28
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AQUEOUS BLOOD GAS CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bionostics, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833146. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUEOUS BLOOD GAS CONTROL?

AQUEOUS BLOOD GAS CONTROL is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Bionostics, Inc.. The 510(k) number is K833146.

When did AQUEOUS BLOOD GAS CONTROL receive FDA 510(k) clearance?

AQUEOUS BLOOD GAS CONTROL received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833146.

Who is the listed applicant for AQUEOUS BLOOD GAS CONTROL?

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

What is the FDA product code for AQUEOUS BLOOD GAS CONTROL?

The FDA product code for AQUEOUS BLOOD GAS CONTROL is JJS.

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Related Devices (Code: JJS)

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K152553CueSee HypoxicEurotrol B.V.K130415HIGH METABOLITE QUALICHECKRadiometer Medical ApsK130236RANGE + QUALICHECK LEVEL 1, RANGE + QUALICHECK LEVEL 2, RANGE + QUALICHECK LEVEL 3Radiometer Medical ApsK033063MISSION CONTROLSDiamond Diagnostics, Inc.K022525LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700 SERIES) LEVELS, 1,2 AND 3, MODEL 507, 508, 509Bio-RadK022529LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL SYNTHESIS SERIES) LEVELS 1,2, AND 3, MODELS 667,668,669Bio-Rad

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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