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SOLCO SILICONE RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874321
510(k) Type
Traditional
Applicant
KAHN-TACT U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
90 days

SOLCO SILICONE RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874321
510(k) Type
Traditional
Applicant
KAHN-TACT U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
90 days