Antrum Needle-Wolf Type
FDA 510(k) K841300 · Popper & Sons, Inc.
510(k) numberK841300
Submission
- Device name
- Antrum Needle-Wolf Type
- Applicant
- Popper & Sons, Inc.
Mchenry, IL, US - Received
- March 30, 1984
- Decision date
- June 5, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Popper & Sons, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K911397 | Hypodermic Needles, Single LumenFCG · Traditional | 05/20/1991SE |
| K843830 | J -Jamshidi Type-Bone Marrow Biopsy/AspiGDM · Traditional | 10/26/1984SE |
| K843690 | Illinois Sternum/Iliac Aspiration NeedleGDM · Traditional | 10/25/1984SE |
| K842406 | Wescott Type Biopsy Needle · Traditional | 08/09/1984SE |
| K841301 | Gardner Type Bone Marrow NeedleGAA · Traditional | 06/05/1984SE |
| K841299 | Bierman Biopsy NeedleGDM · Traditional | 05/02/1984SE |
| K840168 | Westerman-Jensen Biopsy NeedleFCG · Traditional | 03/12/1984SE |
Questions and answers
When was Antrum Needle-Wolf Type cleared by the FDA?
Antrum Needle-Wolf Type (K841300) received a 510(k) decision of Substantially Equivalent on June 5, 1984, 67 days after the submission was received.