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FDA 510(k)

IL 482 CO-OXIMETER

K-Number: K862253 · 1986-07-29

ApplicantInstrumentation Laboratory CO
Decision Date1986-07-29
Product CodeJKS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

IL 482 CO-OXIMETER 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 1986-07-29 under 510(k) number K862253. The device is classified under product code JKS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL 482 CO-OXIMETER?

IL 482 CO-OXIMETER is a medical device that received FDA 510(k) clearance on 1986-07-29. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K862253.

When did IL 482 CO-OXIMETER receive FDA 510(k) clearance?

IL 482 CO-OXIMETER received FDA 510(k) clearance on 1986-07-29, under 510(k) number K862253.

Who is the listed applicant for IL 482 CO-OXIMETER?

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 482 CO-OXIMETER?

The FDA product code for IL 482 CO-OXIMETER is JKS.

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Related Devices (Code: JKS)

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.

K951485AVOXIMETER 4000A-Vox Systems, Inc.K863825CO-OXIMETER SOLUTIONSD.R.G. Scientific IndustriesK853990OSM3 HEMOXIMETERRadiometer America, Inc.K833693TEE ADAPTER 9890-FLUSH WINDING 282Shaban Mfg. Co.K833211BILE SALTS MIXTUREAcumedia Manufacturers, Inc.K832066CONTROL 282Bio-Nustics, Inc.

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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