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 KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI

K-Number: K853242 · 1985-08-30

ApplicantU.S. Mfg. & Management, Inc.
Decision Date1985-08-30
Product Code
DecisionUnknown

Device Summary

I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Mfg. & Management, Inc.. It received FDA 510(k) clearance on 1985-08-30 under 510(k) number K853242. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI?

I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI is a medical device that received FDA 510(k) clearance on 1985-08-30. The listed applicant is U.S. Mfg. & Management, Inc.. The 510(k) number is K853242.

When did I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI receive FDA 510(k) clearance?

I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI received FDA 510(k) clearance on 1985-08-30, under 510(k) number K853242.

Who is the listed applicant for I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI?

The FDA 510(k) record lists U.S. Mfg. & Management, Inc. 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 U.S. Mfg. & Management, 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.

K920860CONTROLLED PASSIVE MOTION MACHINEK874436FLUID SAMPLING PACKK862335MODIFIED I.V. START, RE-START, PEDI AND GERI-KITK842999VENI-SHIELD

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.

↑