Last synced on 14 November 2025 at 11:06 pm

LAPAROSCOPY INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K931778
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1994
Days to Decision
368 days
Submission Type
Summary

LAPAROSCOPY INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K931778
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1994
Days to Decision
368 days
Submission Type
Summary