Last synced on 30 September 2022 at 11:05 pm

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900618
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1990
Days to Decision
76 days

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900618
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1990
Days to Decision
76 days