Last synced on 30 September 2022 at 11:05 pm

OMNI-VENT, SERIES D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872113
510(k) Type
Traditional
Applicant
STEIN-GATES MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1988
Days to Decision
296 days

OMNI-VENT, SERIES D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872113
510(k) Type
Traditional
Applicant
STEIN-GATES MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1988
Days to Decision
296 days