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FDA 510(k)

TUBING CONNECTORS EC-2XXX SERIES

K-Number: K833322 · 1983-12-16

ApplicantGish Biomedical, Inc.
Decision Date1983-12-16
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TUBING CONNECTORS EC-2XXX SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Gish Biomedical, Inc.. It received FDA 510(k) clearance on 1983-12-16 under 510(k) number K833322. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING CONNECTORS EC-2XXX SERIES?

TUBING CONNECTORS EC-2XXX SERIES is a medical device that received FDA 510(k) clearance on 1983-12-16. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K833322.

When did TUBING CONNECTORS EC-2XXX SERIES receive FDA 510(k) clearance?

TUBING CONNECTORS EC-2XXX SERIES received FDA 510(k) clearance on 1983-12-16, under 510(k) number K833322.

Who is the listed applicant for TUBING CONNECTORS EC-2XXX SERIES?

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

What is the FDA product code for TUBING CONNECTORS EC-2XXX SERIES?

The FDA product code for TUBING CONNECTORS EC-2XXX SERIES is DTL.

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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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