(93 days)
No
The description focuses on the mechanical and functional aspects of a guide catheter and does not mention any AI or ML components.
No.
This device is described as an "outer guide catheter" and an "introducer" designed to facilitate the delivery of other devices and contrast medium, rather than directly treating a condition itself.
No
The device is an outer guide catheter used for accessing the venous system of the heart during implantation procedures, delivering other devices and fluids, and serving as a conduit. Its primary functions are interventional and supportive, not diagnostic (i.e., identifying a disease or condition).
No
The device description clearly describes a physical catheter with specific material properties, dimensions, and mechanical features, indicating it is a hardware device, not software.
Based on the provided information, the St. Jude Medical Slittable Direct™ Outer Guide Catheter is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly describes a device used for intracardiac access and delivery of devices and fluids within the venous system of the heart. This is an in vivo application, meaning it is used within a living organism.
- Device Description: The description details a catheter designed to be inserted into the body to cannulate the Coronary Sinus and serve as a conduit. This further supports its use within the body.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (like blood, urine, or tissue) outside of the body to provide information about a patient's health. IVDs are typically used for diagnosis, monitoring, or screening based on analysis of these specimens.
Therefore, the St. Jude Medical Slittable Direct™ Outer Guide Catheter is a medical device used for interventional procedures, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
The St. Jude Medical Slittable Direct™ Outer Guide Catheter is designed for intracardiac access of the venous system of the heart and to serve as a conduit during implantation for the delivery of contrast medium and St. Jude Medical devices, including implantable left heart leads and delivery tools, and support of fluids where minimizing blood loss is essential. In addition, the outer guide catheters can work with inner catheters as a system.
Product codes
DQY
Device Description
The outer catheter is an introducer that is used to cannulate the Coronary Sinus (CS).
The CPS Direct SL outer catheter will have 7 different curves configurations. The catheters will be available in 47 and 54cm working lengths and are radiopaque. The inner diameter of the sheath shall be PTFE lined and to ensure additional lubricity the inside and outside surfaces of the sheath shall be coated with a lubricious coating. The sheath shall have a proximal split away hub which interfaces with the hemostasis valve.
The catheter functions as an outer catheter and can work with an inner guide catheter as a system.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
venous system of the heart
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Device comparison testing was performed to support equivalency of the CPS Direct™ SL Outer Catheter to the predicate devices. Verification was also performed which included mecharical. functional and biocompatibility testing with the CPS Direct meeting all specified design and performance specifications.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Medtronic Attain™ LDS (K021587), Attain Access (K021589), Guidant Rapido™ Cut-Away/Advance (K031505)
Reference Device(s)
Medtronic Attain™ LDS/Access, K042194, K021589, Guidant Rapido™ Cut-Away/Advance, K031505
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 870.1250 Percutaneous catheter.
(a)
Identification. A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.(b)
Classification. Class II (performance standards).
0
FEB 2 4 2006
PREMARKET NOTIFICATION [510(K)] SUMMARY
| Date Prepared: | November 21, 2005 |
|---|---|
| Submitter: | St. Jude Medical, CRMD |
| Address: | 15900 Valley View Court |
| Sylmar, CA 91324 | |
| Phone: | 818 493-2629 |
| Fax: | 818 493-3615 |
| Contact Person: | Deanna Hughes |
| Trade Name/Proprietary Name: | CPS Direct™ SL Outer Catheter |
| Common Name: | Catheter, Percuatenous |
| Classification: | Class II, 21 CFR 870.1250 |
| Legally marketed device | |
| to which your firm is | |
| claiming equivalence: | Medtronic Attain™ LDS (K021587) Attain Access (K021589) |
| Guidant Rapido™ Cut-Away/Advance (K031505) |
Device Description:
I
(
The outer catheter is an introducer that is used to cannulate the Coronary Sinus (CS).
The CPS Direct SL outer catheter will have 7 different curves configurations. The catheters will be available in 47 and 54cm working lengths and are radiopaque. The inner diameter of the sheath shall be PTFE lined and to ensure additional lubricity the inside and outside surfaces of the sheath shall be coated with a lubricious coating. The sheath shall have a proximal split away hub which interfaces with the hemostasis valve.
The catheter functions as an outer catheter and can work with an inner guide catheter as a system.
Intended Use of the Device:
The St. Jude Medical Slittable Direct™ Outer Guide Catheter is designed for intracardiac access of the venous system of the heart and to serve as a conduit during implantation for the delivery of contrast medium and St. Jude Medical devices, including implantable left heart leads and delivery tools, and support of fluids where minimizing blood loss is essential. In addition, the outer guide catheters can work with inner catheters as a system.
CPS Direct™ SL Outer Catheter Traditional 510(k) St. Jude Medical. CRM
Page 14
1
Technological Characteristics of the Device Compared to the Predicate Device:
The CPS Direct™ SL Outer Catheters use similar technology, have similar intended uses, functions, materials and methods of operation as the following predicate devices.
Summary of Studies:
Device comparison testing was performed to support equivalency of the CPS Direct™ SL Outer Catheter to the predicate devices. Verification was also performed which included mecharical. functional and biocompatibility testing with the CPS Direct meeting all specified design and performance specifications.
Biocompatibility Information:
St. Jude Medical has performed biocompatibility testing on the patient tissue contacting materials used in the CPS Direct™ SL Outer Catheter and have been found to be biocompatible.
Sterilization Validation:
The CPS Direct™ SL Outer Catheters are sterilized using a validated Ethylene Oxide (EtO) sterilization process.
Conclusion:
St. Jude Medical considers the CPS Direct™ SL Outer Catheter to be substantially equivalent to the legally marketed predicate and referenced devices. The results of the tests provide reasonable assurance that the device has been designed and tested to assure conformance to the requirements for its indications for use.
CPS Direct™ SL Outer Catheter Traditional 510(k) St. Jude Medical. CRM
2
STATEMENT OF INDICATIONS FOR USE
510(k) Number (if known):
CPS Direct™ SL Outer Catheter Device Name:
Indications for Use:
The St. Jude Medical Slittable Direct™ Outer Guide Catheter is designed for intracardiac The St. Jude Hourself in the heart and to serve as a conduit during implantation for the delivery of contrast medium and St. Jude Medical devices, including implantable left heart leads and delivery tools, and support of fluids where minimizing blood loss is essential. In addition, the outer guide catheters can work with inner catheters as a system.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED) A WIND STATE AND STATE CONSTITUTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSUL
Concurrence of CDRH, Office of Device Evaluation (ODE)
3
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
FEB 2 4 2006
Ms. Deanna L. Hughes Regulatory Affairs St. Jude Medical, CRMD 15900 Valley View Court Sylmar, CA 91342
Re: K053277
Trade Name: CPS Direct™ SL Outer Catheter Regulation Number: 21 CFR 870.1250 Regulation Name: Percutaneous Catheter Regulatory Class: Class II (two) Product Code: DQY Dated: November 21, 2005 Received: November 23, 2005
Dear Ms. Hughes:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
4
Page 2 – Ms. Deanna L. Hughes
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Bram D/ Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
STATEMENT OF INDICATIONS FOR USE
510(k) Number (if known):
CPS Direct™ SL Outer Catheter Device Name:
Indications for Use:
The St. Jude Medical Slittable Direct™ Outer Guide Catheter is designed for intracardiac access of the venous system of the heart and to serve as a conduit during implantation for the delivery of contrast medium and St. Jude Medical devices, including implantable left heart leads and delivery tools, and support of fluids where minimizing blood loss is essential. In addition, the outer guide catheters can work with inner catheters as a system.
Prescription Use X (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
. .
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Wh
(Division/Sig-Off)
Division of Cardiovascular Devices
510(k) Number K053277