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APNEA ALARM FOR ADULT-PEDIATRIC & NEON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831601
510(k) Type
Traditional
Applicant
PLASMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1983
Days to Decision
131 days

APNEA ALARM FOR ADULT-PEDIATRIC & NEON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831601
510(k) Type
Traditional
Applicant
PLASMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1983
Days to Decision
131 days