Last synced on 4 February 2023 at 10:33 pm

M2000 INTRAPARTUM FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823188
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
92 days

M2000 INTRAPARTUM FETAL MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823188
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
92 days