Last synced on 14 November 2025 at 11:06 pm

LACIMAL INTUBATION SETS

Page Type
Cleared 510(K)
510(k) Number
K831901
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
28 days

LACIMAL INTUBATION SETS

Page Type
Cleared 510(K)
510(k) Number
K831901
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
28 days