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LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE

Page Type
Cleared 510(K)
510(k) Number
K880452
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
51 days

LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE

Page Type
Cleared 510(K)
510(k) Number
K880452
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
51 days