Last synced on 14 November 2025 at 11:06 pm

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K915696
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1992
Days to Decision
337 days
Submission Type
Summary

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K915696
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1992
Days to Decision
337 days
Submission Type
Summary