Last synced on 14 June 2024 at 11:05 pm

ENDO I/A PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924149
510(k) Type
Traditional
Applicant
SNOWDEN-PENCER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1993
Days to Decision
161 days
Submission Type
Statement