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FDA 510(k)

IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA

K-Number: K864271 · 1986-11-25

Decision Date1986-11-25
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA 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 1986-11-25 under 510(k) number K864271. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA?

IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K864271.

When did IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA receive FDA 510(k) clearance?

IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA received FDA 510(k) clearance on 1986-11-25, under 510(k) number K864271.

Who is the listed applicant for IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA?

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 TEST 84673-30 CHROMOGENICS CONTROL PLASMA?

The FDA product code for IL TEST 84673-30 CHROMOGENICS CONTROL PLASMA is JPA.

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: JPA)

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.

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