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SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882955
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
561 days

SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882955
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
561 days