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LO-CORE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K882064
510(k) Type
Traditional
Applicant
DEVICE LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
52 days

LO-CORE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K882064
510(k) Type
Traditional
Applicant
DEVICE LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
52 days