Last synced on 20 May 2022 at 11:05 pm

ADULT APNEA MONITOR (20), MONITOR INTERFACE (30)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870835
510(k) Type
Traditional
Applicant
APPLIED MEMBRANE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
24 days

ADULT APNEA MONITOR (20), MONITOR INTERFACE (30)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870835
510(k) Type
Traditional
Applicant
APPLIED MEMBRANE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1987
Days to Decision
24 days