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: K875315 · 1988-02-17

ApplicantNi-Med, Inc.
Decision Date1988-02-17
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. START KITS is the device name listed in this FDA 510(k) record. The listed applicant is Ni-Med, Inc.. It received FDA 510(k) clearance on 1988-02-17 under 510(k) number K875315. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

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 1988-02-17. The listed applicant is Ni-Med, Inc.. The 510(k) number is K875315.

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

I.V. START KITS received FDA 510(k) clearance on 1988-02-17, under 510(k) number K875315.

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

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

What is the FDA product code for I.V. START KITS?

The FDA product code for I.V. START KITS is LRS.

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 Ni-Med, 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.

K981910SUCTION CATHETERK872824P. URINE METER, 250CC

Related Devices (Code: LRS)

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.

K050654AMSINO I.V. START KITAmsino International, Inc.K001879INFUSION IV SETNirvi Intl. USAK963722IV START KITGrand Medical ProductsK951167EMS I.V. START KITEmergency Medical Supply, Inc.K950184B. BRAUN IV START KITSB. Braun of America, Inc.K944041PERSONAL HEARING SYSTEMResound Corp.

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.

↑