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PANDA NEEDLE CATHETER JEJUNOSTOMY KIT

Page Type
Cleared 510(K)
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

PANDA NEEDLE CATHETER JEJUNOSTOMY KIT

Page Type
Cleared 510(K)
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