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FDA 510(k)

CLEAR LEADS-RADIOTRANSPARENT WIRES

K-Number: K834583 · 1984-01-30

ApplicantQuinton, Inc.
Decision Date1984-01-30
Product CodeIKD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLEAR LEADS-RADIOTRANSPARENT WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834583. The device is classified under product code IKD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR LEADS-RADIOTRANSPARENT WIRES?

CLEAR LEADS-RADIOTRANSPARENT WIRES is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Quinton, Inc.. The 510(k) number is K834583.

When did CLEAR LEADS-RADIOTRANSPARENT WIRES receive FDA 510(k) clearance?

CLEAR LEADS-RADIOTRANSPARENT WIRES received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834583.

Who is the listed applicant for CLEAR LEADS-RADIOTRANSPARENT WIRES?

The FDA 510(k) record lists Quinton, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEAR LEADS-RADIOTRANSPARENT WIRES?

The FDA product code for CLEAR LEADS-RADIOTRANSPARENT WIRES is IKD.

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 Quinton, Inc. 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 164 devices →

Related Devices (Code: IKD)

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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