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FDA 510(k)

CENTRACATH #130,135 & 137-HEMOCATH #

K-Number: K833079 · 1983-12-29

ApplicantExco, Inc.
Decision Date1983-12-29
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTRACATH #130,135 & 137-HEMOCATH # is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833079. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRACATH #130,135 & 137-HEMOCATH #?

CENTRACATH #130,135 & 137-HEMOCATH # is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Exco, Inc.. The 510(k) number is K833079.

When did CENTRACATH #130,135 & 137-HEMOCATH # receive FDA 510(k) clearance?

CENTRACATH #130,135 & 137-HEMOCATH # received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833079.

Who is the listed applicant for CENTRACATH #130,135 & 137-HEMOCATH #?

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

What is the FDA product code for CENTRACATH #130,135 & 137-HEMOCATH #?

The FDA product code for CENTRACATH #130,135 & 137-HEMOCATH # is FOZ.

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Related Devices (Code: FOZ)

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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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