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FDA 510(k)

SALINE IV FLUSH SYRINGE

K-Number: K002142 · 2002-01-28

ApplicantEmt-Rx
Decision Date2002-01-28
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SALINE IV FLUSH SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Emt-Rx. It received FDA 510(k) clearance on 2002-01-28 under 510(k) number K002142. 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 SALINE IV FLUSH SYRINGE?

SALINE IV FLUSH SYRINGE is a medical device that received FDA 510(k) clearance on 2002-01-28. The listed applicant is Emt-Rx. The 510(k) number is K002142.

When did SALINE IV FLUSH SYRINGE receive FDA 510(k) clearance?

SALINE IV FLUSH SYRINGE received FDA 510(k) clearance on 2002-01-28, under 510(k) number K002142.

Who is the listed applicant for SALINE IV FLUSH SYRINGE?

The FDA 510(k) record lists Emt-Rx as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SALINE IV FLUSH SYRINGE?

The FDA product code for SALINE IV FLUSH SYRINGE is FOZ.

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Related Devices (Code: FOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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