Last synced on 4 February 2023 at 10:33 pm

MODEL 9000 RECORDING SYSTEM/RESPIRATION MONITORING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860455
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1986
Days to Decision
55 days

MODEL 9000 RECORDING SYSTEM/RESPIRATION MONITORING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860455
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1986
Days to Decision
55 days