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FLEXITE SUPREME, FLEXITE PLUS, FLEXITE M.P., NORTHERN AND FLEXITE PRO-GUARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072479
510(k) Type
Traditional
Applicant
RAPID INJECTION SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2007
Days to Decision
66 days
Submission Type
Statement

FLEXITE SUPREME, FLEXITE PLUS, FLEXITE M.P., NORTHERN AND FLEXITE PRO-GUARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072479
510(k) Type
Traditional
Applicant
RAPID INJECTION SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2007
Days to Decision
66 days
Submission Type
Statement