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FDA 510(k)

IL HEPARINIZED FLOW DIRECTED THERMAL

K-Number: K833836 · 1984-02-04

ApplicantInstrumentation Laboratory CO
Decision Date1984-02-04
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IL HEPARINIZED FLOW DIRECTED THERMAL 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 1984-02-04 under 510(k) number K833836. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL HEPARINIZED FLOW DIRECTED THERMAL?

IL HEPARINIZED FLOW DIRECTED THERMAL is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K833836.

When did IL HEPARINIZED FLOW DIRECTED THERMAL receive FDA 510(k) clearance?

IL HEPARINIZED FLOW DIRECTED THERMAL received FDA 510(k) clearance on 1984-02-04, under 510(k) number K833836.

Who is the listed applicant for IL HEPARINIZED FLOW DIRECTED THERMAL?

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 HEPARINIZED FLOW DIRECTED THERMAL?

The FDA product code for IL HEPARINIZED FLOW DIRECTED THERMAL is DYG.

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Other records listing Instrumentation Laboratory CO as applicant

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Related Devices (Code: DYG)

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.

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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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