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FDA 510(k)

INJECTOR

K-Number: K023737 · 2003-07-14

ApplicantAnton Meyer & Co. , Ltd.
Decision Date2003-07-14
Product CodeMSS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Anton Meyer & Co. , Ltd.. It received FDA 510(k) clearance on 2003-07-14 under 510(k) number K023737. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTOR?

INJECTOR is a medical device that received FDA 510(k) clearance on 2003-07-14. The listed applicant is Anton Meyer & Co. , Ltd.. The 510(k) number is K023737.

When did INJECTOR receive FDA 510(k) clearance?

INJECTOR received FDA 510(k) clearance on 2003-07-14, under 510(k) number K023737.

Who is the listed applicant for INJECTOR?

The FDA 510(k) record lists Anton Meyer & Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECTOR?

The FDA product code for INJECTOR is MSS.

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 PubMed Literature

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.

PMID: 38645777Risks and benefits associated with the primary functions of artificial intelligence powered autoinjectors.Frontiers in medical technology ()PMID: 38130421Framework for creating a qualified medical device development tool of autoinjectors.Frontiers in medical technology ()

Related Devices (Code: MSS)

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.

K261174RxSight® Insertion DeviceRxsight, Inc.K252540ACCUJECT Injector Set 2.1-1P (LP604590)Medicel AGK242389EyeGility™ Inserter for Preloaded enVista IOLsBausch & Lomb, IncorporatedK231106Accuject Refra Injector AR2900Medicel AGK231838RxSight® Insertion Device (63002)Rxsight, Inc.K231466RxSight Insertion DeviceRxsight, Inc.

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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