Intermedics Cyberlith I Unipolar Cardiac
FDA 510(k) K810384 · Intermedics, Inc.
510(k) numberK810384
Submission
- Device name
- Intermedics Cyberlith I Unipolar Cardiac
- Applicant
- Intermedics, Inc.
Mchenry, IL, US - Received
- February 13, 1981
- Decision date
- February 13, 1981
- Decision
- Unknown (SESP)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Intermedics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K954610 | Model 430-07 Endocardial Pacing LeadDTB · Traditional | 12/16/1996PT |
| K955122 | Intermedics Model 436-07 Bipolar & Model 437-07 Unipolar Implantable Endocardial Pacing…DTB · Traditional | 11/04/1996ST |
| K962174 | Biplr Im En Pac Leads (430-07,432-03,436-02 & 07, 438-05 & 07)DTB · Traditional | 08/21/1996ST |
| K955550 | Cardifix Ez Bipolar/Unipolar Endocardial Pacing LeadDTB · Traditional | 06/19/1996ST |
| K960281 | Implantable Pacing Leads/Implantable Accessory/Non-Implantable AccessoryDTB · Traditional | 06/18/1996ST |
| K954719 | Intermedics Model 430-07 Bipolar Implantable Endocardial Pacing LeadDTB · Traditional | 02/27/1996ST |
| K933278 | Intermedics Triangle Chest Probe Model 526-04KRG · Traditional | 03/15/1995SE |
| K922042 | Cardifix Endocardial Pacing LeadDTB · Traditional | 04/29/1993SESP |
| K922972 | Models 438-05 and 435-05 Implantable Pacing LeadDTB · Traditional | 01/22/1993SESP |
| K920530 | Intermedics Model 366-15 VS 1 Header PlugDXY · Traditional | 03/17/1992SE |
Questions and answers
When was Intermedics Cyberlith I Unipolar Cardiac cleared by the FDA?
Intermedics Cyberlith I Unipolar Cardiac (K810384) received a 510(k) decision of Unknown on February 13, 1981, 0 days after the submission was received.