Last synced on 14 June 2024 at 11:05 pm

RETRACTORS, SPECULUM, CLIP APPLIER FOR TITANIUM CLIPS, 2-WAY STOP COCK, PALPATION PROBE, KNOT GUIDE, ROEDER LOOP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936250
510(k) Type
Traditional
Applicant
MEDICON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1994
Days to Decision
133 days
Submission Type
Summary