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FDA 510(k)

HEPARIN LOCK FLUSH SYRINGE

K-Number: K032417 · 2003-12-23

ApplicantAm2 Pat, Inc.
Decision Date2003-12-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEPARIN LOCK FLUSH SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Am2 Pat, Inc.. It received FDA 510(k) clearance on 2003-12-23 under 510(k) number K032417. 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 HEPARIN LOCK FLUSH SYRINGE?

HEPARIN LOCK FLUSH SYRINGE is a medical device that received FDA 510(k) clearance on 2003-12-23. The listed applicant is Am2 Pat, Inc.. The 510(k) number is K032417.

When did HEPARIN LOCK FLUSH SYRINGE receive FDA 510(k) clearance?

HEPARIN LOCK FLUSH SYRINGE received FDA 510(k) clearance on 2003-12-23, under 510(k) number K032417.

Who is the listed applicant for HEPARIN LOCK FLUSH SYRINGE?

The FDA 510(k) record lists Am2 Pat, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEPARIN LOCK FLUSH SYRINGE?

The FDA product code for HEPARIN LOCK FLUSH SYRINGE is 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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