FDA 510(k) clearance · back to tracker

ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable

Acist Medical Systems, Inc. cleared K252653 on 2026-05-13, decision: substantially equivalent

K-number

K252653

Sponsor

Acist Medical Systems, Inc.

Device

ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-05-13

Product code

DXT

Advisory committee

Cardiovascular

Medical specialty

Cardiovascular

Regulation number

870.1650

Official FDA record

Open K252653on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K252653 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.