Last synced on 20 December 2024 at 11:05 pm

INFANT NASAL CANNULAE ASSEMBLY, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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