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iSchemaView RAPID

Page Type
Cleared 510(K)
510(k) Number
K182130
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2018
Days to Decision
143 days
Submission Type
Summary

iSchemaView RAPID

Page Type
Cleared 510(K)
510(k) Number
K182130
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2018
Days to Decision
143 days
Submission Type
Summary