Last synced on 14 November 2025 at 11:06 pm

ZYLOX

Page Type
Cleared 510(K)
510(k) Number
K782139
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1979
Days to Decision
56 days

ZYLOX

Page Type
Cleared 510(K)
510(k) Number
K782139
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1979
Days to Decision
56 days