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AMNIPERF(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926425
510(k) Type
Traditional
Applicant
RAYMART DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
439 days
Submission Type
Statement

AMNIPERF(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926425
510(k) Type
Traditional
Applicant
RAYMART DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
439 days
Submission Type
Statement