ClearanceBrief
Company ยท US

Aqua Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2019 to 2025. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 8, 2025K251226Aqua Medical RF Vapor Ablation System
Aqua Medical, Inc.
KNS
Dec 12, 2024K241271Aqua Medical RF Vapor Ablation System
Aqua Medical, Inc.
KNS
Dec 17, 2021K213627RF Vapor System
Aqua Medical, Inc.
KNS
May 27, 2021K211282Aqua Medical RF Vapor System
Aqua Medical, Inc.
KNS
Jun 21, 2019K183595Aqua Medical RF Vapor System
Aqua Medical, Inc.
KNS

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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