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Data / Medical devices / United States / Vacumed, Div. Of Vacumetrics, Inc.

Vacumed, Div. Of Vacumetrics, Inc.: FDA-registered device maker in Ventura, CA, United States, 5 510(k) clearances

Vacumed, Div. Of Vacumetrics, Inc. is registered with the FDA (registration 2023529) in Ventura, CA, United States. It lists 10 device types. The FDA files 5 510(k) clearances under its listings, the newest dated May 26, 1998. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
2023529
Address
6085 King Dr Unit 104, Ventura, CA, United States, 93003
Owner or operator
VACUMED, DIV. OF VACUMETRICS, INC. (2023529)
Roles
Manufacturer, Repackager or relabeler, Specification developer
First device listed
October 7, 1992
Registered through
2026
Brand names listed
VACUMED, Vacumed

Devices it lists

DeviceProduct codeClassRoleSource
Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2Manufactureraccessdata.fda.gov
Analyzer, Gas, Oxygen, Gaseous-PhaseCCL2Manufactureraccessdata.fda.gov
Calculator, Pulmonary Function DataBZC2Manufactureraccessdata.fda.gov
Calculator, Pulmonary Function Interpretor (Diagnostic)BZM2Manufactureraccessdata.fda.gov
Clip, NoseBXJ1Specification developeraccessdata.fda.gov
Computer, Oxygen-UptakeBZL2Manufactureraccessdata.fda.gov
Mouthpiece, BreathingBYP1Repackager or relabeleraccessdata.fda.gov
Set, Tubing And Support, Ventilator (W Harness)BZO1Repackager or relabeleraccessdata.fda.gov
Strap, Head, Gas MaskBTK1Repackager or relabeleraccessdata.fda.gov
Tubing, Pressure And AccessoriesBYX1Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 26, 1998K973545VACU*MED GOLD EDITION OXYGEN GAS ANALYZERCCLSubstantially EquivalentVacumed, Div. of Vacumetrics, Inc.accessdata.fda.gov
May 26, 1998K973544VACU*MED, GOLD EDITION CARBON DIOXIDE GAS ANALYZERCCKSubstantially EquivalentVacumed, Div. of Vacumetrics, Inc.accessdata.fda.gov
March 4, 1987K864852VISTA INTERFACE SYSTEMBZLSubstantially EquivalentVacumetrics, Inc.accessdata.fda.gov
April 2, 1986K860844VISTA INTERFACE SYSSTEMBZCSubstantially EquivalentVacumetrics, Inc.accessdata.fda.gov
May 3, 1985K851706UNIVERSAL COMPUTER INTERFACE SYSTEMBZMSubstantially EquivalentVacumetrics, Inc.accessdata.fda.gov

Compare with other makers

Updated May 26, 1998. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.