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OMNI-VENT, SERIES D/MRI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881420
510(k) Type
Traditional
Applicant
STEIN-GATES MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1988
Days to Decision
71 days

OMNI-VENT, SERIES D/MRI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881420
510(k) Type
Traditional
Applicant
STEIN-GATES MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1988
Days to Decision
71 days