Last synced on 14 November 2025 at 11:06 pm

ACKERMANN EUROPCLIP

Page Type
Cleared 510(K)
510(k) Number
K111930
510(k) Type
Traditional
Applicant
ACKERMANN INSTRUMENTE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2011
Days to Decision
124 days
Submission Type
Summary

ACKERMANN EUROPCLIP

Page Type
Cleared 510(K)
510(k) Number
K111930
510(k) Type
Traditional
Applicant
ACKERMANN INSTRUMENTE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2011
Days to Decision
124 days
Submission Type
Summary