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FDA 510(k)

RAAF DUAL LUMEN CATHETER

K-Number: K822849 · 1982-11-29

ApplicantQuinton, Inc.
Decision Date1982-11-29
Product Code
DecisionSubstantially Equivalent

Device Summary

RAAF DUAL LUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1982-11-29 under 510(k) number K822849. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAAF DUAL LUMEN CATHETER?

RAAF DUAL LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 1982-11-29. The listed applicant is Quinton, Inc.. The 510(k) number is K822849.

When did RAAF DUAL LUMEN CATHETER receive FDA 510(k) clearance?

RAAF DUAL LUMEN CATHETER received FDA 510(k) clearance on 1982-11-29, under 510(k) number K822849.

Who is the listed applicant for RAAF DUAL LUMEN CATHETER?

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

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.

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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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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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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