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)

NON STERILE PARENTERAL SUPPLY KIT

K-Number: K900857 · 1990-05-22

ApplicantIntermed, Inc.
Decision Date1990-05-22
Product CodeFMF
Advisory CommitteeHO
DecisionUnknown

Device Summary

NON STERILE PARENTERAL SUPPLY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Intermed, Inc.. It received FDA 510(k) clearance on 1990-05-22 under 510(k) number K900857. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NON STERILE PARENTERAL SUPPLY KIT?

NON STERILE PARENTERAL SUPPLY KIT is a medical device that received FDA 510(k) clearance on 1990-05-22. The listed applicant is Intermed, Inc.. The 510(k) number is K900857.

When did NON STERILE PARENTERAL SUPPLY KIT receive FDA 510(k) clearance?

NON STERILE PARENTERAL SUPPLY KIT received FDA 510(k) clearance on 1990-05-22, under 510(k) number K900857.

Who is the listed applicant for NON STERILE PARENTERAL SUPPLY KIT?

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

What is the FDA product code for NON STERILE PARENTERAL SUPPLY KIT?

The FDA product code for NON STERILE PARENTERAL SUPPLY KIT 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 Intermed, 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.

K842166INTERMED, INS STERILE WATER/SALINEK833126DRESSING CHANGE TRAYSK833573CENTRAL VEIN CATH. TRAY CC-20-1420K833574PERCUTANEOUS SHEATH INTRODUCER TRAYSK833139ACUTE HEMODIALYSIS TRAYSK833059SUCTION CATHETER TRAYS

View all 16 devices →

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.

↑