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ACMI ASPIRATOR KIT #8808

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811218
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1981
Days to Decision
58 days

ACMI ASPIRATOR KIT #8808

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811218
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1981
Days to Decision
58 days