Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ANESTHESIA INJECTION TOOL SET

K-Number: K113247 · 2012-03-27

ApplicantKi Works Co., Ltd.
Decision Date2012-03-27
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA INJECTION TOOL SET is the device name listed in this FDA 510(k) record. The listed applicant is Ki Works Co., Ltd.. It received FDA 510(k) clearance on 2012-03-27 under 510(k) number K113247. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA INJECTION TOOL SET?

ANESTHESIA INJECTION TOOL SET is a medical device that received FDA 510(k) clearance on 2012-03-27. The listed applicant is Ki Works Co., Ltd.. The 510(k) number is K113247.

When did ANESTHESIA INJECTION TOOL SET receive FDA 510(k) clearance?

ANESTHESIA INJECTION TOOL SET received FDA 510(k) clearance on 2012-03-27, under 510(k) number K113247.

Who is the listed applicant for ANESTHESIA INJECTION TOOL SET?

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

What is the FDA product code for ANESTHESIA INJECTION TOOL SET?

The FDA product code for ANESTHESIA INJECTION TOOL SET is EJI.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: EJI)

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.

K171254LeEject 2 Dental Syringe and Needle SystemAdvanced Technology and Capital, Inc.K120659HU-FRIEDY DENTAL CARTRIDGE SYRINGEHu-Friedy Mfg. Co., LLCK082249MORPHEUSMeibach Tech LtdaK092943ASPIRATING SYRINGE, NON-ASPIRATING SYRINGEArnold Tuber IndustriesK083796MILTEX ASPIRATING SYRINGE, MILTEX PETITE ASPIRATING SYRINGE, MILTEX SELF-ASPIRATING SYRINGE, MILTEX LIGHTWEIGHTMiltex, Inc.K081694DENJECTORDxm Co., 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.

↑