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FDA 510(k)

ORIGIN FLEXIBLE PORT

K-Number: K922751 · 1992-11-20

ApplicantOrigin Medsystems, Inc.
Decision Date1992-11-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ORIGIN FLEXIBLE PORT is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1992-11-20 under 510(k) number K922751. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORIGIN FLEXIBLE PORT?

ORIGIN FLEXIBLE PORT is a medical device that received FDA 510(k) clearance on 1992-11-20. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K922751.

When did ORIGIN FLEXIBLE PORT receive FDA 510(k) clearance?

ORIGIN FLEXIBLE PORT received FDA 510(k) clearance on 1992-11-20, under 510(k) number K922751.

Who is the listed applicant for ORIGIN FLEXIBLE PORT?

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

What is the FDA product code for ORIGIN FLEXIBLE PORT?

The FDA product code for ORIGIN FLEXIBLE PORT is GCJ.

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Related Devices (Code: GCJ)

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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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