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MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

Page Type
Cleared 510(K)
510(k) Number
K900731
510(k) Type
Traditional
Applicant
MEDICAL CONSULTANTS INTL. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1990
Days to Decision
305 days

MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

Page Type
Cleared 510(K)
510(k) Number
K900731
510(k) Type
Traditional
Applicant
MEDICAL CONSULTANTS INTL. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1990
Days to Decision
305 days