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PANDA NEEDLE CATHETER JEJUNOSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921127
510(k) Type
Traditional
Applicant
KNIGHT MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
1/4/1993
Days to Decision
300 days
Submission Type
Statement