← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

DRE — Dilator, Vessel, For Percutaneous Catheterization

DEVICE CLASS
Class II
REGULATION
21 CFR 870.1310
MEDICAL SPECIALTY
Cardiovascular
REVIEW PANEL
CV
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES

Recent clearances

K253616Sorin Group Italia S.R.L. · 510k2025-12-19
K251325Baylis Medical Company, Inc. · 510k2025-05-29
K242229Merit Medical Systems, Inc. · 510k2025-01-15

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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