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FDA 510(k)

ULTICARE SAFETY INSULIN SYRINGE

K-Number: K103011 · 2011-02-02

Decision Date2011-02-02
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTICARE SAFETY INSULIN SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 2011-02-02 under 510(k) number K103011. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTICARE SAFETY INSULIN SYRINGE?

ULTICARE SAFETY INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 2011-02-02. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K103011.

When did ULTICARE SAFETY INSULIN SYRINGE receive FDA 510(k) clearance?

ULTICARE SAFETY INSULIN SYRINGE received FDA 510(k) clearance on 2011-02-02, under 510(k) number K103011.

Who is the listed applicant for ULTICARE SAFETY INSULIN SYRINGE?

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

What is the FDA product code for ULTICARE SAFETY INSULIN SYRINGE?

The FDA product code for ULTICARE SAFETY INSULIN SYRINGE is MEG.

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 Ulti-Med Intl., 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 21 devices →

Related Devices (Code: MEG)

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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