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BEECHER 20 GA. PROBE

Page Type
Cleared 510(K)
510(k) Number
K833800
510(k) Type
Traditional
Applicant
BEECHER MEDICAL DIAGNOSTIC INSTRUMENTATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1984
Days to Decision
65 days

BEECHER 20 GA. PROBE

Page Type
Cleared 510(K)
510(k) Number
K833800
510(k) Type
Traditional
Applicant
BEECHER MEDICAL DIAGNOSTIC INSTRUMENTATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1984
Days to Decision
65 days