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FDA 510(k)

AQUEOUS PH/BLOOD GAS CONTROLS

K-Number: K770228 · 1977-06-27

ApplicantInstrumentation Laboratory CO
Decision Date1977-06-27
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AQUEOUS PH/BLOOD GAS CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1977-06-27 under 510(k) number K770228. 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 PH/BLOOD GAS CONTROLS?

AQUEOUS PH/BLOOD GAS CONTROLS is a medical device that received FDA 510(k) clearance on 1977-06-27. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K770228.

When did AQUEOUS PH/BLOOD GAS CONTROLS receive FDA 510(k) clearance?

AQUEOUS PH/BLOOD GAS CONTROLS received FDA 510(k) clearance on 1977-06-27, under 510(k) number K770228.

Who is the listed applicant for AQUEOUS PH/BLOOD GAS CONTROLS?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUEOUS PH/BLOOD GAS CONTROLS?

The FDA product code for AQUEOUS PH/BLOOD GAS CONTROLS is JJS.

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Related Devices (Code: JJS)

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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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