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HI-TEMP LOOPTIP SURGICAL CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K802330
510(k) Type
Traditional
Applicant
MEDICAL PRODUCTS DEVELOPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
50 days

HI-TEMP LOOPTIP SURGICAL CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K802330
510(k) Type
Traditional
Applicant
MEDICAL PRODUCTS DEVELOPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
50 days