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FDA 510(k)

IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST

K-Number: K913927 · 1991-10-11

ApplicantInstrumentation Laboratory CO
Decision Date1991-10-11
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST 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 1991-10-11 under 510(k) number K913927. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST?

IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST is a medical device that received FDA 510(k) clearance on 1991-10-11. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K913927.

When did IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST receive FDA 510(k) clearance?

IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST received FDA 510(k) clearance on 1991-10-11, under 510(k) number K913927.

Who is the listed applicant for IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST?

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 IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST?

The FDA product code for IL BG3 SYST, MODEL 1420, BLOOD GAS & PH TEST SYST is CHL.

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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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