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QUALITONE ULTRA CANAL GENESIS

Page Type
Cleared 510(K)
510(k) Number
K904730
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1990
Days to Decision
51 days

QUALITONE ULTRA CANAL GENESIS

Page Type
Cleared 510(K)
510(k) Number
K904730
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1990
Days to Decision
51 days