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FLORET NEURO SPONGE

Page Type
Cleared 510(K)
510(k) Number
K830269
510(k) Type
Traditional
Applicant
RITMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
128 days

FLORET NEURO SPONGE

Page Type
Cleared 510(K)
510(k) Number
K830269
510(k) Type
Traditional
Applicant
RITMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
128 days