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SINGLE USE NEEDLE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K780975
510(k) Type
Traditional
Applicant
ASPEN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1978
Days to Decision
13 days

SINGLE USE NEEDLE ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K780975
510(k) Type
Traditional
Applicant
ASPEN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1978
Days to Decision
13 days