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FDA 510(k)

COMPACT AUTO-SAFETY INJECTOR (CASI)

K-Number: K073476 · 2008-03-07

ApplicantMedical House (Asi) Limited
Decision Date2008-03-07
Product CodeKZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMPACT AUTO-SAFETY INJECTOR (CASI) is the device name listed in this FDA 510(k) record. The listed applicant is Medical House (Asi) Limited. It received FDA 510(k) clearance on 2008-03-07 under 510(k) number K073476. The device is classified under product code KZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPACT AUTO-SAFETY INJECTOR (CASI)?

COMPACT AUTO-SAFETY INJECTOR (CASI) is a medical device that received FDA 510(k) clearance on 2008-03-07. The listed applicant is Medical House (Asi) Limited. The 510(k) number is K073476.

When did COMPACT AUTO-SAFETY INJECTOR (CASI) receive FDA 510(k) clearance?

COMPACT AUTO-SAFETY INJECTOR (CASI) received FDA 510(k) clearance on 2008-03-07, under 510(k) number K073476.

Who is the listed applicant for COMPACT AUTO-SAFETY INJECTOR (CASI)?

The FDA 510(k) record lists Medical House (Asi) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPACT AUTO-SAFETY INJECTOR (CASI)?

The FDA product code for COMPACT AUTO-SAFETY INJECTOR (CASI) is KZH.

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.

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Related Devices (Code: KZH)

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.

K243232GripMateSynthon Hispania S.L.K213429AccuSert Needle InserterEmed Technologies CorporationK163400Orbit InserterYpsomed AGK160860MiniMed Quick-serterMedtronic MinimedK124026LOBSTER AUTO-INJECTORScandinavian Health LimitedK122837AUTOJECT 2 FOR GLASSY SYRINGEOwen Mumford, Ltd.

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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