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FDA 510(k)

COBE CENTRY 2000 RX

K-Number: K820125 · 1982-03-23

ApplicantCobe Laboratories, Inc.
Decision Date1982-03-23
Product Code
DecisionSubstantially Equivalent

Device Summary

COBE CENTRY 2000 RX 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 1982-03-23 under 510(k) number K820125. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBE CENTRY 2000 RX?

COBE CENTRY 2000 RX is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K820125.

When did COBE CENTRY 2000 RX receive FDA 510(k) clearance?

COBE CENTRY 2000 RX received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820125.

Who is the listed applicant for COBE CENTRY 2000 RX?

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

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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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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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