Gas Insufflator— 510(k) K221995

Name: FDA 510(k) clearance K221995
Creator: U.S. Food and Drug Administration
Published: 2023-03-28

Substantially Equivalent

Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.

FDA 510(k) clearance K221995 for Gas Insufflator, Substantially Equivalent on 2023-03-28. Applicant: Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. Device class: 2.

Clearance details

Applicant: Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.
Product code: Code HIF
Device class: Class 2
Regulation: 21 CFR 884.1730
Advisory panel: Obstetrics/Gynecology
Date received: 2022-07-06
Decision date: 2023-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cixi, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIF

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K260209 — ENDOFLATOR+; Smart Smoke Evacuation2026-08-19
K252584 — Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)2026-06-25
K252318 — Insufflator (OPTO-IFL1000)2026-04-16
K250388 — ENDOFLATOR +2025-09-22
K242772 — AirSurgN Insufflator (10030/AirSurgN)2025-04-11

More clearances from Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.

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K240376 — Electroporation System (N3000)2024-10-04
K212614 — Ultrasonic Scalpel System2022-07-18
K210488 — Ultrasonic Surgical & Electrosurgical Generator2021-10-25
K210116 — Video Endoscopy System, 3D Video Endoscopy System2021-10-13
K183153 — Microwave Ablation System2019-07-08

Adverse events under product code HIF

product code HIF

Death: 19
Injury: 578
Malfunction: 5,639
Total: 6,236

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.