Last synced on 14 November 2025 at 11:06 pm

PROGUARD(TM) BLOOD COLLECTION NEEDLE

Page Type
Cleared 510(K)
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)
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