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)

DAXOR MAX100 SYRINGE (MAX100)

K-Number: K970419 · 1997-12-22

ApplicantDaxor Corporation
Decision Date1997-12-22
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DAXOR MAX100 SYRINGE (MAX100) is the device name listed in this FDA 510(k) record. The listed applicant is Daxor Corporation. It received FDA 510(k) clearance on 1997-12-22 under 510(k) number K970419. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAXOR MAX100 SYRINGE (MAX100)?

DAXOR MAX100 SYRINGE (MAX100) is a medical device that received FDA 510(k) clearance on 1997-12-22. The listed applicant is Daxor Corporation. The 510(k) number is K970419.

When did DAXOR MAX100 SYRINGE (MAX100) receive FDA 510(k) clearance?

DAXOR MAX100 SYRINGE (MAX100) received FDA 510(k) clearance on 1997-12-22, under 510(k) number K970419.

Who is the listed applicant for DAXOR MAX100 SYRINGE (MAX100)?

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

What is the FDA product code for DAXOR MAX100 SYRINGE (MAX100)?

The FDA product code for DAXOR MAX100 SYRINGE (MAX100) is FMF.

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

Other records listing Daxor Corporation 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.

K261099Blood Volume Analyzer (200)K251087Blood Volume Analyzer (200)K964406AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER

Related Devices (Code: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., 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.

↑