Last synced on 14 November 2025 at 11:06 pm

SUPER 6

Page Type
Cleared 510(K)
510(k) Number
K002300
510(k) Type
Traditional
Applicant
DENTAL ALLOY PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2000
Days to Decision
60 days
Submission Type
Statement

SUPER 6

Page Type
Cleared 510(K)
510(k) Number
K002300
510(k) Type
Traditional
Applicant
DENTAL ALLOY PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2000
Days to Decision
60 days
Submission Type
Statement