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LAPAROSCOPY SETS, NEEDLE HOLDERS, BLUNT SHEARS

Page Type
Cleared 510(K)
510(k) Number
K923259
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/1994
Days to Decision
648 days
Submission Type
Statement

LAPAROSCOPY SETS, NEEDLE HOLDERS, BLUNT SHEARS

Page Type
Cleared 510(K)
510(k) Number
K923259
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/1994
Days to Decision
648 days
Submission Type
Statement