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)

I.V. START KITS

K-Number: K864693 · 1986-12-16

ApplicantSalt Creek Medical Technologies
Decision Date1986-12-16
Product Code
DecisionSubstantially Equivalent

Device Summary

I.V. START KITS is the device name listed in this FDA 510(k) record. The listed applicant is Salt Creek Medical Technologies. It received FDA 510(k) clearance on 1986-12-16 under 510(k) number K864693. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. START KITS?

I.V. START KITS is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is Salt Creek Medical Technologies. The 510(k) number is K864693.

When did I.V. START KITS receive FDA 510(k) clearance?

I.V. START KITS received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864693.

Who is the listed applicant for I.V. START KITS?

The FDA 510(k) record lists Salt Creek Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

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 Salt Creek Medical Technologies 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.

K864683NEONATAL FEEDING KITK871042URINE METER, 250CCK871087S.C.M.T. PERFORATORK871075SCMT UMBILICAL CLAMPK864296S.C.T. MULTI PORT, INJECTION SITEK864682SALT CREEK P.I. TRAY

View all 8 devices →

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.

↑