Last synced on 21 June 2024 at 11:04 pm

MEDIVISION LAPAROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984434
510(k) Type
Traditional
Applicant
MEDIVISION SCOPE SERVICE CENTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1999
Days to Decision
93 days
Submission Type
Statement