Breast Lesion Localization Needle
FDA 510(k) K944942 · Promedical , Ltd.
510(k) numberK944942
Submission
- Device name
- Breast Lesion Localization Needle
- Applicant
- Promedical , Ltd.
Wyckoff, NJ, US - Received
- October 7, 1994
- Decision date
- November 4, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GDF – Guide, Needle, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code GDF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K031173 | Needletech Guidewire Introducer Needle, Models 40021, 40069, 40053, 40042 & 40013GDF · Traditional | Needle Tech Products, Inc. | 07/23/2003SE |
| K950311 | Global Medical Products Brest Lesion Localization Needle with Stiffened WireGDF · Traditional | Global Medical Products, Ltd. | 05/26/1995SE |
| K950007 | Surgical Instrument GuideGDF · Traditional | United States Surgical, A Division of Tyco Healthc | 03/15/1995SE |
| K945124 | Breast Lesion Localization NeedleGDF · Traditional | Promex, Inc. | 11/22/1994SE |
| K935538 | Bauer Temno Coaxial NeedleGDF · Traditional | Bauer Medical, Inc. | 02/22/1994SE |
| K935457 | Localization Wire or Marker - SurgicalGDF · Traditional | Bip USA, Inc. | 02/17/1994SE |
| K923840 | Needle-GrabberGDF · Traditional | Guardian Angel Products, Inc. | 07/13/1993SE |
| K923835 | The Eleventh FingerGDF · Traditional | Guardian Angel Products, Inc. | 07/09/1993SE |
| K925875 | Horizontal Needle Guide AttachmentGDF · Traditional | Bip USA, Inc. | 04/06/1993SE |
| K924270 | Breast Lesion Localization NeedleGDF · Traditional | Core Medical, Inc. | 09/23/1992SE |
More from Core Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K954596 | Pro-B Core-Rect Coaxial Biopsy SystemFCG · Traditional | 10/07/1995SE |
| K952350 | Jamshidi Style Biopsy Needle (Acri) (Biomid), Illinois Style Biopsy Needle (Isan)LWE · Traditional | 07/17/1995SE |
| K951598 | Pro-B Biopsy NeedleFCG · Traditional | 04/21/1995SE |
| K944944 | Chiba, Franseen, Westcott, Spinal Style Aspiration Biopsy NeedleFCG · Traditional | 12/21/1994SE |
Questions and answers
When was Breast Lesion Localization Needle cleared by the FDA?
Breast Lesion Localization Needle (K944942) received a 510(k) decision of Substantially Equivalent on November 4, 1994, 28 days after the submission was received.
What is the product code of K944942?
The FDA product code is GDF – Guide, Needle, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4800.