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MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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