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FDA 510(k)

COBE CLOSED WOUND DRAINAGE KIT

K-Number: K902759 · 1990-07-18

ApplicantCobe Laboratories, Inc.
Decision Date1990-07-18
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COBE CLOSED WOUND DRAINAGE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Laboratories, Inc.. It received FDA 510(k) clearance on 1990-07-18 under 510(k) number K902759. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBE CLOSED WOUND DRAINAGE KIT?

COBE CLOSED WOUND DRAINAGE KIT is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K902759.

When did COBE CLOSED WOUND DRAINAGE KIT receive FDA 510(k) clearance?

COBE CLOSED WOUND DRAINAGE KIT received FDA 510(k) clearance on 1990-07-18, under 510(k) number K902759.

Who is the listed applicant for COBE CLOSED WOUND DRAINAGE KIT?

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

What is the FDA product code for COBE CLOSED WOUND DRAINAGE KIT?

The FDA product code for COBE CLOSED WOUND DRAINAGE KIT is CAC.

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Other records listing Cobe Laboratories, Inc. as applicant

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K923272COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATORK900105COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTICK905793COBE CENTRY 2 BICART OPTION KITK905388COBE CENTRYSYSTEM 3 BICART OPTION KITK904336NEW COBE SATURATION/HEMATOCRIT MONITORK902631COBE ICU CONVERSION KIT

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Related Devices (Code: CAC)

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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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