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FDA 510(k)

CHEST DRAINAGE TUBING

K-Number: K993062 · 1999-12-10

ApplicantOlson Medical Sales, Inc.
Decision Date1999-12-10
Product CodeDWE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHEST DRAINAGE TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Olson Medical Sales, Inc.. It received FDA 510(k) clearance on 1999-12-10 under 510(k) number K993062. The device is classified under product code DWE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEST DRAINAGE TUBING?

CHEST DRAINAGE TUBING is a medical device that received FDA 510(k) clearance on 1999-12-10. The listed applicant is Olson Medical Sales, Inc.. The 510(k) number is K993062.

When did CHEST DRAINAGE TUBING receive FDA 510(k) clearance?

CHEST DRAINAGE TUBING received FDA 510(k) clearance on 1999-12-10, under 510(k) number K993062.

Who is the listed applicant for CHEST DRAINAGE TUBING?

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

What is the FDA product code for CHEST DRAINAGE TUBING?

The FDA product code for CHEST DRAINAGE TUBING is DWE.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Olson Medical Sales, 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.

K000977COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT - HEAT EXCHANGER COILSK993060GAS FILTERK992906COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT

Related Devices (Code: DWE)

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.

K233702SMARxT Tubing and ConnectorsLivaNova USA, Inc.K092486VORTEX MEDICAL ANGIOVAC CARDIOPULMONARY BYPASS CIRCUITVortex Medical, Inc.K080592HLM TUBING SET WITH BIOLINE COATINGMaquet Cardiopulmonary, AGK053025JOSTRA HLM TUBING SETMaquet Cardiopulmonary, AGK022857PUMP TUBING WITH X-COATINGTerumo Cardiovascular Systems CorporationK013578PUMP TUBINGTerumo Cardiovascular Systems Corp.

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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