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PROGUARD(TM) BLOOD COLLECTION NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904295
510(k) Type
Traditional
Applicant
SAFETY-JECT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1990
Days to Decision
26 days

PROGUARD(TM) BLOOD COLLECTION NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904295
510(k) Type
Traditional
Applicant
SAFETY-JECT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1990
Days to Decision
26 days