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FDA 510(k)

IL 7F FLOW DIRECTOR THERMAL DILU. CATH

K-Number: K820702 · 1982-04-21

Decision Date1982-04-21
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IL 7F FLOW DIRECTOR THERMAL DILU. CATH 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 1982-04-21 under 510(k) number K820702. 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 7F FLOW DIRECTOR THERMAL DILU. CATH?

IL 7F FLOW DIRECTOR THERMAL DILU. CATH is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K820702.

When did IL 7F FLOW DIRECTOR THERMAL DILU. CATH receive FDA 510(k) clearance?

IL 7F FLOW DIRECTOR THERMAL DILU. CATH received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820702.

Who is the listed applicant for IL 7F FLOW DIRECTOR THERMAL DILU. CATH?

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 7F FLOW DIRECTOR THERMAL DILU. CATH?

The FDA product code for IL 7F FLOW DIRECTOR THERMAL DILU. CATH is DYG.

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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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