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FDA 510(k)

EXEL I.V. EXTENSION SET

K-Number: K092172 · 2010-01-04

Decision Date2010-01-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXEL I.V. EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Exelint Intl. Co.. It received FDA 510(k) clearance on 2010-01-04 under 510(k) number K092172. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXEL I.V. EXTENSION SET?

EXEL I.V. EXTENSION SET is a medical device that received FDA 510(k) clearance on 2010-01-04. The listed applicant is Exelint Intl. Co.. The 510(k) number is K092172.

When did EXEL I.V. EXTENSION SET receive FDA 510(k) clearance?

EXEL I.V. EXTENSION SET received FDA 510(k) clearance on 2010-01-04, under 510(k) number K092172.

Who is the listed applicant for EXEL I.V. EXTENSION SET?

The FDA 510(k) record lists Exelint Intl. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXEL I.V. EXTENSION SET?

The FDA product code for EXEL I.V. EXTENSION SET is FPA.

Related Clinical Trials

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.

Other records listing Exelint Intl. Co. as applicant

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.

View all 12 devices →

Related Devices (Code: FPA)

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.

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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