Last synced on 14 November 2025 at 11:06 pm

SHARPLAN MODEL 712 ACUSPOT MICROMANIPULATOR

Page Type
Cleared 510(K)
510(k) Number
K951204
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1995
Days to Decision
76 days
Submission Type
Summary

SHARPLAN MODEL 712 ACUSPOT MICROMANIPULATOR

Page Type
Cleared 510(K)
510(k) Number
K951204
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1995
Days to Decision
76 days
Submission Type
Summary