Modified Keymed Flexible Esophageal Dilators
FDA 510(k) K881478 · Keymed (Medical & Industrial Equipment), Ltd.
510(k) numberK881478
Submission
- Device name
- Modified Keymed Flexible Esophageal Dilators
- Applicant
- Keymed (Medical & Industrial Equipment), Ltd.
Essex, GB - Received
- April 6, 1988
- Decision date
- September 14, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KNQ – Dilator, Esophageal
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5365
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code KNQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K122924 | Cre Fixed Wire Ballon Dilation CatheterKNQ · Special | Boston Scientific Corp | 10/24/2012SE |
| K093236 | Ethicon Endo-Surgeryoptical DilatorKNQ · Special | Ethicon Endo-Surgery, Inc. | 11/10/2009SE |
| K090183 | Hercules 3 Stage Wire Guided Dilation BalloonKNQ · Special | Cook Endoscopy | 09/25/2009SE |
| K082995 | Smart DilatorKNQ · Traditional | Safestitch Medical | 02/06/2009SE |
| K061937 | Cook Endoscopy Esophageal Dilation BalloonKNQ · Traditional | Cook Endoscopy | 12/01/2006SE |
| K061787 | Maxforce TTS Single-Use Balloon DilatorKNQ · Traditional | Boston Scientific Corp | 09/21/2006SE |
| K060302 | Inscope Precision Balloon Dilator - Wire GuidedKNQ · Traditional | Cordis Europa, N.V. | 04/11/2006SE |
| K043605 | Inscope 3-STAGE Balloon DilatorKNQ · Traditional | Cordis Europa, N.V. | 02/04/2005SE |
| K033936 | Bard Eliminator PET Balloon DilatorsKNQ · Special | C.R. Bard, Inc. | 01/14/2004SE |
| K031147 | Optical DVS (Dual Vector Shearing) Esophageal DilatorKNQ · Traditional | Ethicon Endo-Surgery, Inc. | 01/12/2004SE |
More from Ethicon Endo-Surgery, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K100899 | Olympus Endoscopic Flushing Pump, Model OPF-2FEQ · Traditional | 09/13/2010SE |
| K011725 | Olympus Suction Pump, Model KV-5JCX · Traditional | 08/31/2001SE |
| K000948 | Olympus Endoscopic Flushing Pump Model OFP-1FEQ · Traditional | 05/12/2000SE |
| K962528 | Olympus Mobile Chair/CouchFZK · Traditional | 12/12/1996SE |
| K930852 | Olympus Suction Pump Model KV-4JCX · Traditional | 03/31/1994SE |
Questions and answers
When was Modified Keymed Flexible Esophageal Dilators cleared by the FDA?
Modified Keymed Flexible Esophageal Dilators (K881478) received a 510(k) decision of Substantially Equivalent on September 14, 1988, 161 days after the submission was received.
What is the product code of K881478?
The FDA product code is KNQ – Dilator, Esophageal, a Class II (moderate risk) device regulated under 21 CFR 876.5365.