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MODIFIED INFANT NASAL CANNULAE ASSEMBLY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895031
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1989
Days to Decision
83 days

MODIFIED INFANT NASAL CANNULAE ASSEMBLY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895031
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1989
Days to Decision
83 days