HYCULT DIAMOND CORONARY BYPASS KNIFE
FDA 510(k) clearance K900379 · decided 1990-03-19
Clearance details
- K-number
- K900379
- Device name
- HYCULT DIAMOND CORONARY BYPASS KNIFE
- Applicant
- St. Jude Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-01-26
- Decision date
- 1990-03-19
- Days to decision
- 52 days
- Clearance type
- Traditional
- Product code
- DWS
- Device class
- 1
- Regulation number
- 870.4500
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- St. Paul, MN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch St. Jude Medical
The Builder collects up to 8 candidate devices side by side with yours, then exports the substantial-equivalence comparison scaffold. How it works
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626 (K022238) | Medtronic Vascular | 2002-10-09 |
| OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006) (K964445) | Dlp, Inc. | 1997-01-30 |
| BURKE CONGENITAL THORACOSCOPY INSTRUMENTS (K962771) | Pilling Weck, Inc. | 1996-11-19 |
| RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY (K955689) | Contour Fabricators of Florida, Inc. | 1996-05-15 |
| G.E. STERILE ANGIOGRAPHIC TRAY (K960139) | GE Medical Systems | 1996-04-19 |
| G.E. STERILE CT BIOPSY TRAY (K960144) | GE Medical Systems | 1996-04-15 |
| G.E. STERILE DIGITAL ANGIOGRAPHIC TRAY (K960143) | GE Medical Systems | 1996-04-09 |
| REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER (K934727) | Cardiac Pacemakers, Inc. | 1994-01-10 |
| INSULATION PAD (K896307) | Bio-Vascular, Inc. | 1990-01-19 |
| MODEL 6888 LEAD TUNNELER (K894738) | Cardiac Pacemakers, Inc. | 1989-09-13 |
| NEWCHILL(TM) CARDIAC INSULATOR (K892804) | Acacia Laboratories, Inc. | 1989-07-14 |
| MODIFIED STERILIZATION METHOD OF PTI HEART-LIFT (K893436) | Pioneering Technologies, Inc. | 1989-07-14 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS (P880006/S094) | St. Jude Medical, Inc. | 2016-02-12 |
| SENSOLOG / DIALOG/ REGENCY FAMILY OF PACEMAKERS (P880006/S093) | St. Jude Medical, Inc. | 2015-08-27 |
| SESOLOG / DIALOG / REGENCY FAMILY OF PACEMAKERS (P880006/S092) | St. Jude Medical, Inc. | 2015-02-25 |
| SENSOLOG/ DIALOG/REGENCY FAMILY OF PACEMAKERS (P880006/S089) | St. Jude Medical, Inc. | 2014-09-12 |
| SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS (P880006/S088) | St. Jude Medical, Inc. | 2014-05-29 |
| SENSOLOG/ DIALOG/REGENCY FAMILY OF PACEMAKERS (P880006/S081) | St. Jude Medical, Inc. | 2014-04-10 |
| SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS (P880006/S085) | St. Jude Medical, Inc. | 2014-03-20 |
| SENSOLOG/DIALOG/ REGENCY FAMILY OF PACEMAKERS (P880006/S087) | St. Jude Medical, Inc. | 2014-02-26 |