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KPE 220 TS, NONSTERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914221
510(k) Type
Traditional
Applicant
IPAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1991
Days to Decision
63 days
Submission Type
Statement

KPE 220 TS, NONSTERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914221
510(k) Type
Traditional
Applicant
IPAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1991
Days to Decision
63 days
Submission Type
Statement