Last synced on 14 November 2025 at 11:06 pm

EIM-107 PREP-CHECK

Page Type
Cleared 510(K)
510(k) Number
K993202
510(k) Type
Traditional
Applicant
General Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
84 days
Submission Type
Statement

EIM-107 PREP-CHECK

Page Type
Cleared 510(K)
510(k) Number
K993202
510(k) Type
Traditional
Applicant
General Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1999
Days to Decision
84 days
Submission Type
Statement