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)

LABORATORY DATA MGMT SYSTEM SDMS

K-Number: K831838 · 1984-01-24

ApplicantVickers America Medical Corp.
Decision Date1984-01-24
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LABORATORY DATA MGMT SYSTEM SDMS is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1984-01-24 under 510(k) number K831838. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABORATORY DATA MGMT SYSTEM SDMS?

LABORATORY DATA MGMT SYSTEM SDMS is a medical device that received FDA 510(k) clearance on 1984-01-24. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K831838.

When did LABORATORY DATA MGMT SYSTEM SDMS receive FDA 510(k) clearance?

LABORATORY DATA MGMT SYSTEM SDMS received FDA 510(k) clearance on 1984-01-24, under 510(k) number K831838.

Who is the listed applicant for LABORATORY DATA MGMT SYSTEM SDMS?

The FDA 510(k) record lists Vickers America Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LABORATORY DATA MGMT SYSTEM SDMS?

The FDA product code for LABORATORY DATA MGMT SYSTEM SDMS is JQP.

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 Vickers America Medical Corp. 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.

K840823TREONIC C30K830748RESUSCITAIREK830936TREONIC IP5K813239OXYGENAIRE NURING INCUBATORK813238NEOCARE BABY-CONTROLLED INCUBATORK811865VMA PEDIATRIC APNEA MATTRESS

View all 22 devices →

Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, Inc.

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.

↑