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FDA 510(k)

MULTI-4 CO-OXIMETER CONTROL

K-Number: K861901 · 1986-06-17

ApplicantAllied Instrumentation Laboratory
Decision Date1986-06-17
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTI-4 CO-OXIMETER CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Allied Instrumentation Laboratory. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K861901. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-4 CO-OXIMETER CONTROL?

MULTI-4 CO-OXIMETER CONTROL is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Allied Instrumentation Laboratory. The 510(k) number is K861901.

When did MULTI-4 CO-OXIMETER CONTROL receive FDA 510(k) clearance?

MULTI-4 CO-OXIMETER CONTROL received FDA 510(k) clearance on 1986-06-17, under 510(k) number K861901.

Who is the listed applicant for MULTI-4 CO-OXIMETER CONTROL?

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

What is the FDA product code for MULTI-4 CO-OXIMETER CONTROL?

The FDA product code for MULTI-4 CO-OXIMETER CONTROL is JJY.

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Other records listing Allied Instrumentation Laboratory as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K860365PHENOBARBITAL TEST SYSTEMK860286IL TEST PHENYTOINK853858IL TEST THEOPHYLLINE ASSAYK852676IL SYSTEM 1304 & 1306, PH/BLOOD GAS ANALYZERSK851933CLINICAL CHEMISTRY ANALYTICAL SYSTEMK850748I-L TEST, DIRECT BILIRUBIN SET

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Related Devices (Code: JJY)

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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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