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FDA 510(k)

ISECURE SYRINGE CARTRIDGE HOLDER

K-Number: K063180 · 2006-12-11

ApplicantHospira, Inc.
Decision Date2006-12-11
Product CodeIQG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ISECURE SYRINGE CARTRIDGE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2006-12-11 under 510(k) number K063180. The device is classified under product code IQG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISECURE SYRINGE CARTRIDGE HOLDER?

ISECURE SYRINGE CARTRIDGE HOLDER is a medical device that received FDA 510(k) clearance on 2006-12-11. The listed applicant is Hospira, Inc.. The 510(k) number is K063180.

When did ISECURE SYRINGE CARTRIDGE HOLDER receive FDA 510(k) clearance?

ISECURE SYRINGE CARTRIDGE HOLDER received FDA 510(k) clearance on 2006-12-11, under 510(k) number K063180.

Who is the listed applicant for ISECURE SYRINGE CARTRIDGE HOLDER?

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

What is the FDA product code for ISECURE SYRINGE CARTRIDGE HOLDER?

The FDA product code for ISECURE SYRINGE CARTRIDGE HOLDER is IQG.

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 Hospira, Inc. 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 36 devices →

Related Devices (Code: IQG)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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