Endo Cervical Curette
FDA 510(k) K926532 · Thomasville Medical Assoc.
510(k) numberK926532
Submission
- Device name
- Endo Cervical Curette
- Applicant
- Thomasville Medical Assoc.
Alpharetta, GA, US - Received
- December 30, 1992
- Decision date
- February 25, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- KNA – Instrument, Manual, Specialized Obstetric-Gynecologic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.4530
- Specialty
- Obstetrics/Gynecology
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| K130087 | Panpac Word/Bartholin CatheterKNA · Traditional | Panpac Medical Corporation | 01/10/2014SE |
| K102141 | Cook Word Bartholin Gland Catheter (Final Trade Name Not Yet Determined)KNA · Traditional | Cook Urological, Inc. | 05/06/2011SE |
| K093904 | Glenveigh Vaginal Tamponade Balloon CatheterKNA · Traditional | Glenveigh Surgical, LLC | 04/14/2010SE |
| K082939 | Cook Fetal Membrane Manipulator, Model -FMM-122400KNA · Traditional | Cook Urological, Inc. | 09/03/2009SE |
| K062438 | Bakri Postpartum Balloon, Model J-SOS-100500KNA · Traditional | Cook Ob/Gyn | 10/27/2006SE |
| K060289 | Epistat, V-Stat, Models EPISTAT-001-01, V-STAT-001-01KNA · Traditional | Frontline Medical | 07/07/2006SE |
| K013597 | Tamponade Uterine Balloon Catheter SetKNA · Traditional | Cook Ob/Gyn | 04/17/2002SE |
| K014248 | DND 202 Manual Urological Digital Needle DriverKNA · Traditional | Urogyn , Ltd. | 03/21/2002SE |
| K001590 | DND 101KNA · Traditional | Urogyn , Ltd. | 08/02/2000SE |
| K990738 | Dr. Jahanger's CutterKNA · Traditional | M.S. Jahanger, MD | 10/29/1999SE |
More from M.S. Jahanger, MD
| 510(k) | Device | Decision |
|---|---|---|
| K926429 | Vaginal Specula: Cusco, Guttman, InfantHDF · Traditional | 02/28/1994SE |
| K930030 | Suction Tubes: House, BaronJCX · Traditional | 02/25/1994SE |
| K926540 | Sopher and Bierer Ovum ForcepsHLZ · Traditional | 02/25/1994SE |
| K926536 | Disposable Plastic Vaginal SpeculaHIB · Traditional | 02/25/1994SE |
| K926535 | Gomco Circumcision ClampHFX · Traditional | 02/25/1994SE |
| K926533 | Z-Clamp ForcepsHCZ · Traditional | 02/25/1994SE |
| K926531 | Hysterectomy ForcepsHCZ · Traditional | 02/25/1994SE |
| K926527 | Roto Fit Biopsy ForcepsHFB · Traditional | 02/25/1994SE |
| K926484 | Corson Myoma Grasping ForcepsHCZ · Traditional | 02/25/1994SE |
| K926471 | Mogan Circumcision ClampHFX · Traditional | 02/25/1994SE |
Questions and answers
When was Endo Cervical Curette cleared by the FDA?
Endo Cervical Curette (K926532) received a 510(k) decision of Substantially Equivalent on February 25, 1994, 422 days after the submission was received.
What is the product code of K926532?
The FDA product code is KNA – Instrument, Manual, Specialized Obstetric-Gynecologic, a Class II (moderate risk) device regulated under 21 CFR 884.4530.