FDA 510(k) clearance · back to tracker

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set

Cerenovus, Inc. cleared K251828 on 2025-08-22, decision: substantially equivalent

K-number

K251828

Sponsor

Cerenovus, Inc.

Device

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set

Class

Class II

Decision

Substantially Equivalent

Decision date

2025-08-22

Product code

NRY

Advisory committee

Cardiovascular

Medical specialty

Cardiovascular

Regulation number

870.1250

Official FDA record

Open K251828on accessdata.fda.gov →

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

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Raw record →

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

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Source

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