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FDA 510(k)

DUAL PORT ENTERAL Y-ADAPTOR

K-Number: K923168 · 1994-06-17

ApplicantOrion Life Systems, Inc.
Decision Date1994-06-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUAL PORT ENTERAL Y-ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Orion Life Systems, Inc.. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K923168. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL PORT ENTERAL Y-ADAPTOR?

DUAL PORT ENTERAL Y-ADAPTOR is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Orion Life Systems, Inc.. The 510(k) number is K923168.

When did DUAL PORT ENTERAL Y-ADAPTOR receive FDA 510(k) clearance?

DUAL PORT ENTERAL Y-ADAPTOR received FDA 510(k) clearance on 1994-06-17, under 510(k) number K923168.

Who is the listed applicant for DUAL PORT ENTERAL Y-ADAPTOR?

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

What is the FDA product code for DUAL PORT ENTERAL Y-ADAPTOR?

The FDA product code for DUAL PORT ENTERAL Y-ADAPTOR is KNT.

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Related Devices (Code: KNT)

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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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