Last synced on 14 November 2025 at 11:06 pm

PERIOTEST

Page Type
Cleared 510(K)
510(k) Number
K872171
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1987
Days to Decision
15 days

PERIOTEST

Page Type
Cleared 510(K)
510(k) Number
K872171
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1987
Days to Decision
15 days