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EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800456
510(k) Type
Traditional
Applicant
KHI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1980
Days to Decision
18 days

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800456
510(k) Type
Traditional
Applicant
KHI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1980
Days to Decision
18 days