Last synced on 6 December 2024 at 11:05 pm

ACKERMANN SURGICAL INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974382
510(k) Type
Traditional
Applicant
ACKERMANN INSTRUMENTE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1998
Days to Decision
151 days
Submission Type
Summary