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ClenchGuard

Page Type
Cleared 510(K)
510(k) Number
K181005
510(k) Type
Traditional
Applicant
Boyd Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2020
Days to Decision
639 days
Submission Type
Statement

ClenchGuard

Page Type
Cleared 510(K)
510(k) Number
K181005
510(k) Type
Traditional
Applicant
Boyd Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2020
Days to Decision
639 days
Submission Type
Statement