← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
DSA — Cable, Transducer And Electrode, Patient, (Including Connector)
DEVICE CLASS
Class II
REGULATION
21 CFR 870.2900
MEDICAL SPECIALTY
Cardiovascular
REVIEW PANEL
CV
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
5
510(K)/PMA CLEARANCES
510k: 5
0
RECALL ENTRIES
Recent clearances
K254114Baylis Medical Technologies, Inc. · 510k2026-01-18
K252827Drägerwerk AG & Co. KGaA · 510k2025-12-01
K251669Shanghai Draeger Medical Instrument Co., Ltd. · 510k2025-09-30
K242986Beijing Rongrui-Century Science & Technology Co., Ltd. · 510k2025-05-02
K243545Philips Medizin Systeme Böblingen GmbH · 510k2025-01-17
Related on SPEQ
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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