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INFANT NASAL CANNULAE ASSEMBLY, MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K911780
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1991
Days to Decision
63 days
Submission Type
Statement

INFANT NASAL CANNULAE ASSEMBLY, MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K911780
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1991
Days to Decision
63 days
Submission Type
Statement