ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Ca
Summary
Acist Medical Systems, Inc. received 510(k) clearance for ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable, a DXT device. Cleared on 2026-05-13.
Details
Source
510(k) Clearance
External ID
K252653
Action Date
2026-05-13
Status
Traditional
Category
device
Product Code
DXT
Product Description
ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable. Product code: DXT.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Acist Medical Systems, Inc. has received 3 total clearances in our database.
Acist Medical Systems, Inc. has 3 FDA actions in our database, including 3 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Acist Medical Systems, Inc. have FDA actions?
Acist Medical Systems, Inc. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252653" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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