PERCOR STAT-DL 9.5 FR. 34 & 40CC
Device Facts
| Record ID | K960166 |
|---|---|
| Device Name | PERCOR STAT-DL 9.5 FR. 34 & 40CC |
| Applicant | Datascope Corp. |
| Product Code | DSP · Cardiovascular |
| Decision Date | Apr 24, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.3535 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Intended Use
The intra-aortic balloon is placed in the descending aorta just below the subclavian artery and is intended to improve cardiovascular functioning during the following situations: Refractory ventricular failure, Cardiogenic shock, Unstable angina, Unstable refractory angina, Impending infarction, Septic shock, Cardiac support for high risk surgical patients, Ischemic related intractable ventricular arrhythmias, Mechanical complications due to acute myocardial infarction.
Device Story
Intra-aortic balloon (IAB) catheter; placed in descending aorta below subclavian artery; provides mechanical circulatory support. Device functions via inflation/deflation cycle to improve cardiovascular hemodynamics. Used in clinical settings (e.g., OR, ICU) by trained medical professionals. Subject device modification involves alternate inner lumen material grade/composition compared to predicate. Output is mechanical cardiac assistance; assists in stabilizing patients with acute cardiac conditions.
Clinical Evidence
No clinical data. Bench testing only.
Technological Characteristics
Intra-aortic balloon catheter; 9.5Fr diameter. Modification involves alternate material grade and chemical composition for the inner lumen. Mechanical device; no energy source or software.
Indications for Use
Indicated for patients experiencing refractory ventricular failure, cardiogenic shock, unstable angina, unstable refractory angina, impending infarction, septic shock, need for cardiac support during high-risk surgery, ischemic-related intractable ventricular arrhythmias, or mechanical complications due to acute myocardial infarction.
Regulatory Classification
Identification
An intra-aortic balloon and control system is a prescription device that consists of an inflatable balloon, which is placed in the aorta to improve cardiovascular functioning during certain life-threatening emergencies, and a control system for regulating the inflation and deflation of the balloon. The control system, which monitors and is synchronized with the electrocardiogram, provides a means for setting the inflation and deflation of the balloon with the cardiac cycle.
Special Controls
*Classification.* (1) Class II (special controls) when the device is indicated for acute coronary syndrome, cardiac and non-cardiac surgery, or complications of heart failure. The special controls for this device are:(i) Appropriate analysis and non-clinical testing must be conducted to validate electromagnetic compatibility and electrical safety of the device; (ii) Software verification, validation, and hazard analysis must be performed; (iii) The device must be demonstrated to be biocompatible; (iv) Sterility and shelf-life testing must demonstrate the sterility of patient-contacting components and the shelf life of these components; (v) Non-clinical performance evaluation of the device must demonstrate mechanical integrity, durability, and reliability to support its intended purpose; and (vi) Labeling must include a detailed summary of the device- and procedure-related complications pertinent to use of the device. (2) Class III (premarket approval) when the device is indicated for septic shock and pulsatile flow generation. (c) *Date premarket approval application (PMA) or notice of completion of product development protocol (PDP) is required.* A PMA or notice of completion of a PDP is required to be filed with the Food and Drug Administration on or before March 31, 2014, for any intra-aortic balloon and control system indicated for septic shock or pulsatile flow generation that was in commercial distribution before May 28, 1976, or that has, on or before March 31, 2014, been found to be substantially equivalent to any intra-aortic balloon and control system indicated for septic shock or pulsatile flow generation that was in commercial distribution before May 28, 1976. Any other intra-aortic balloon and control system indicated for septic shock or pulsatile flow generation shall have an approved PMA or declared completed PDP in effect before being placed in commercial distribution.
Predicate Devices
- Datascope Percor STAT-DL® 9.5Fr. Intra-Aortic Balloon (K905056, K940178)
Related Devices
- K091449 — DATASCOPE'S 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MODELS 0684,00-0498-01, 02 · Datascope Corp., Cardiac Assist Division · Jun 18, 2009
- K013326 — MODIFICATION TO: DATASCOPE 8FR. POLYIMIDE ALT B IAB, 25CC, 34CC, 40CC, DATASCOPE INSERTION KIT FOR 8 FR, POLYIMIDE ALT B · Datascope Corp. · Nov 2, 2001
- K980780 — DATASCOPE PERCOR STAT-DL 9.5 FR. 25, 34 AND 40CC INTRA-AORIC BALLOONS WITH ALTERNATE B MEMBRANE FOR OPTIONAL SHEATHLES · Datascope Corp. · May 29, 1998
- K964987 — DATASCOPE PERCOR STAT - DL 9.5 FR. 25 AND 40CC INTRA-AORTIC BALLOON FOR OPTIONAL SHEATHLESS INSERTION AND PERCOR STAT -0 · Datascope Corp. · Mar 17, 1997
- K041281 — DATASCOPE 7.5FR. IAB CATHETER AND ACCESSORIES · Datascope Corp. · Jun 7, 2004
