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FDA 510(k)

MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM

K-Number: K062302 · 2006-10-06

ApplicantMillicore AB
Decision Date2006-10-06
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Millicore AB. It received FDA 510(k) clearance on 2006-10-06 under 510(k) number K062302. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM?

MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-06. The listed applicant is Millicore AB. The 510(k) number is K062302.

When did MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM receive FDA 510(k) clearance?

MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM received FDA 510(k) clearance on 2006-10-06, under 510(k) number K062302.

Who is the listed applicant for MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM?

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

What is the FDA product code for MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM?

The FDA product code for MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM is KDQ.

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Related Devices (Code: KDQ)

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.

K081718EXPRESS CHEST DRAINAtrium Medical Corp.K043582OCEAN CHEST DRAINAtrium Medical Corp.K984496ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAINAtrium Medical Corp.K962856PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTRDeknatel, Inc.K961287ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEMRocket Medical PlcK962168MUCUS SPECIMEN TRAPSage Products, Inc.

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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