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RHYTIDOMETER

Page Type
Cleared 510(K)
510(k) Number
K801939
510(k) Type
Traditional
Applicant
AZTEC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
45 days

RHYTIDOMETER

Page Type
Cleared 510(K)
510(k) Number
K801939
510(k) Type
Traditional
Applicant
AZTEC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
45 days