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FDA 510(k)

INTERTIP INFUSION SET

K-Number: K934204 · 1994-02-07

ApplicantOasis Medical, Inc.
Decision Date1994-02-07
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INTERTIP INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Oasis Medical, Inc.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K934204. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERTIP INFUSION SET?

INTERTIP INFUSION SET is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Oasis Medical, Inc.. The 510(k) number is K934204.

When did INTERTIP INFUSION SET receive FDA 510(k) clearance?

INTERTIP INFUSION SET received FDA 510(k) clearance on 1994-02-07, under 510(k) number K934204.

Who is the listed applicant for INTERTIP INFUSION SET?

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

What is the FDA product code for INTERTIP INFUSION SET?

The FDA product code for INTERTIP INFUSION SET is HQE.

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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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