← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

DQD — Stethoscope, Electronic

DEVICE CLASS
Class II
REGULATION
21 CFR 870.1875
MEDICAL SPECIALTY
Cardiovascular
REVIEW PANEL
CV
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
8
510(K)/PMA CLEARANCES
510k: 8
0
RECALL ENTRIES

Recent clearances

K252915Ai Health Highway India Pvt., Ltd. · 510k2026-05-22
K252089Tyto Care , Ltd. · 510k2026-03-12
K252076Kneevoice, Inc. · 510k2026-02-06
K252284Csd Labs · 510k2025-12-19
K252595Sparrow Acoustics, Inc. · 510k2025-09-12
K251494Eko Health, Inc. · 510k2025-08-12
K242971Heroic Faith International , Ltd. · 510k2024-11-25
K240901Sparrow Acoustics, Inc. · 510k2024-09-19

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.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →