FDA 510(k) clearance · back to tracker
Radio Frequency Ablation System
Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. cleared K190052 on 2019-06-25, decision: substantially equivalent
K-number
K190052
Sponsor
Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.
Device
Radio Frequency Ablation System
Class
Class II
Decision
Substantially Equivalent
Decision date
2019-06-25
Product code
GEI
Advisory committee
General, Plastic Surgery
Medical specialty
General, Plastic Surgery
Regulation number
878.4400
Official FDA record
Open K190052on 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 K190052 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.
Try the sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.