Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IL 1302 PH BLOOD GAS ANALYZER

K-Number: K821483 · 1982-06-10

Decision Date1982-06-10
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL 1302 PH BLOOD GAS ANALYZER 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 1982-06-10 under 510(k) number K821483. 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 1302 PH BLOOD GAS ANALYZER?

IL 1302 PH BLOOD GAS ANALYZER is a medical device that received FDA 510(k) clearance on 1982-06-10. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K821483.

When did IL 1302 PH BLOOD GAS ANALYZER receive FDA 510(k) clearance?

IL 1302 PH BLOOD GAS ANALYZER received FDA 510(k) clearance on 1982-06-10, under 510(k) number K821483.

Who is the listed applicant for IL 1302 PH BLOOD GAS ANALYZER?

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 1302 PH BLOOD GAS ANALYZER?

The FDA product code for IL 1302 PH BLOOD GAS ANALYZER is CHL.

Related Clinical Trials

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.

Other records listing Instrumentation Laboratory CO 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.

View all 315 devices →

Related Devices (Code: CHL)

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.

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.

↑