Last synced on 30 September 2022 at 11:05 pm

INFANT APNEA MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802710
510(k) Type
Traditional
Applicant
DOUGLAS SCIENTIFIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
12 days

INFANT APNEA MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802710
510(k) Type
Traditional
Applicant
DOUGLAS SCIENTIFIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
12 days