(86 days)
Not Found
No
The summary describes a physical medical device (a guiding catheter) and does not mention any software, algorithms, or data processing that would indicate the use of AI or ML.
No.
The intended use states it provides a pathway for therapeutic and diagnostic devices, but it is not a therapeutic device itself.
No
The "Intended Use / Indications for Use" states that the device is intended to "provide a pathway through which therapeutic and diagnostic devices are introduced." This means it is an access device, not a diagnostic device itself.
No
The device description clearly describes a physical catheter, which is a hardware component.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is for providing a pathway to introduce therapeutic and diagnostic devices into the body. IVDs are used to examine specimens outside the body (in vitro) to obtain information about a patient's health.
- Device Description: The description details a physical catheter designed for insertion into the body, not for analyzing biological samples.
- Lack of IVD Characteristics: There is no mention of reagents, assays, sample analysis, or any other typical components or processes associated with in vitro diagnostics.
This device is a medical device used for interventional procedures, specifically a guiding catheter.
N/A
Intended Use / Indications for Use
The ACS VIKING™ Guiding Catheter is intended to provide a pathway through which therapeutic and diagnostic devices are introduced.
Product codes (comma separated list FDA assigned to the subject device)
74 DQY
Device Description
The ACS VIKING™ Guiding Catheter is available in five diameters. The catheter has a standard length of 100 cm, but can be produced in lengths from 40 to 160 cm. The ACS VIKING™ Guiding Catheter is available in varying tip shapes. The guiding catheter has a radiopaque shaft, which varies in stiffness at the distal end. The catheter has a radiopaque soft tip and is available with or without side holes.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
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
Image /page/0/Picture/0 description: The image shows a sequence of alphanumeric characters, seemingly handwritten. The sequence appears to be 'K072424', with some characters slightly distorted or stylized. The characters are written in a dark color, contrasting with the lighter background.
SEP 2 6
510(k) Summary ACS VIKING™ Guiding Catheter
-
- Device Name: ACS VIKING™ Guiding Catheter
-
- Devices to which Equivalence is Claimed: ACS TOURGUIDE™ Coronary Guiding Catheter (K953987)
-
- Indication: The ACS VIKING™ Guiding Catheter is intended to provide a pathway through which therapeutic and diagnostic devices are introduced.
-
- Device Description: The ACS VIKING™ Guiding Catheter is available in five diameters. The catheter has a standard length of 100 cm, but can be produced in lengths from 40 to 160 cm. The ACS VIKING™ Guiding Catheter is available in varying tip shapes. The guiding catheter has a radiopaque shaft, which varies in stiffness at the distal end. The catheter has a radiopaque soft tip and is available with or without side holes.
-
- Summary of Substantial Equivalence: The indications, methods and conditions of use, packaging process and location, sterilization process and location, and bench test results of the subject device are identical to those of the currently marketed ACS TOURGUIDE™ Coronary Guiding Catheter (K953987). Moreover, the two catheters are similar in design and are composed of materials which have undergone biocompatibility testing showing acceptability for clinical use.
-
- Conclusion: The ACS VIKING™ Guiding Catheter is substantially equivalent to the currently marketed ACS TOURGUIDE™ Coronary Guiding Catheter (K953987).
1
Image /page/1/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of a human figure with three overlapping profiles, representing the department's focus on health and human well-being. The logo is simple and recognizable, conveying the department's mission and purpose.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
SEP 2 6 1997
Mr. Judith P. Palin Guidant Corporation Advanced Cardiovascular Systems 3200 Lakeside Drive P.O. Box 58167 Santa Clara, California 95052-8167
Re: K972484 ACS VIKING™ Guiding Catheter Requlatory Class: II (two) Product Code: 74 DQY Dated: July 1, 1997 Received: July 2, 1997
Dear Ms. Palin:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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 (Premarket Approval), 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 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
2
Page 2 - Ms. Judith P. Palin
This letter will allow you to begin marketing your device as described in your 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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4639. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled,
"Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours,
Thomas J. Callahon
Thomas J. Callahan, Ph.D. Director Division of Cardiovascular, Respiratory, and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
Page
510(k) Number (if known): K972484
Device Name: ACS VIKING Tm Guiding Catheter
Indications For Use: The ACS VIKING TH Guiding Catheter is intended to provide a pathway through which therapeutic and diagnostic devices are introduced.
Th AR.
(Division Sign-Off): Division or Cardiovascular, Respiratory, ang Maga Pogical De 51 . . . Mumber
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use
(Per 21 CFR 801.109) $\checkmark$
CR
Over-The-Counter Use__________________________________________________________________________________________________________________________________________________________
(Optional Format 1-2-96)
一、
l