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SNYDER HEMOVAC TM VENTED WOUND KIT

Page Type
Cleared 510(K)
510(k) Number
K800577
510(k) Type
Traditional
Applicant
SNYDER LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1980
Days to Decision
33 days

SNYDER HEMOVAC TM VENTED WOUND KIT

Page Type
Cleared 510(K)
510(k) Number
K800577
510(k) Type
Traditional
Applicant
SNYDER LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1980
Days to Decision
33 days