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NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

Page Type
Cleared 510(K)
510(k) Number
K924931
510(k) Type
Traditional
Applicant
LPC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1993
Days to Decision
229 days
Submission Type
Statement

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

Page Type
Cleared 510(K)
510(k) Number
K924931
510(k) Type
Traditional
Applicant
LPC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1993
Days to Decision
229 days
Submission Type
Statement