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FDA 510(k)

COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER

K-Number: K902671 · 1990-07-17

ApplicantCobe Laboratories, Inc.
Decision Date1990-07-17
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER 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 1990-07-17 under 510(k) number K902671. 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 AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER?

COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER is a medical device that received FDA 510(k) clearance on 1990-07-17. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K902671.

When did COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER receive FDA 510(k) clearance?

COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER received FDA 510(k) clearance on 1990-07-17, under 510(k) number K902671.

Who is the listed applicant for COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER?

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 AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER?

The FDA product code for COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER is CAC.

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Other records listing Cobe Laboratories, 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.

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)

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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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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