SUNTOUCH EYE SPEAR— 510(k) K132796
Substantially EquivalentHuizhou Foryou Medical Devices Co., Ltd.
FDA 510(k) clearance K132796 for SUNTOUCH EYE SPEAR, Substantially Equivalent on 2013-10-30. Applicant: Huizhou Foryou Medical Devices Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Huizhou Foryou Medical Devices Co., Ltd.
- Product code
- Code HOZ
- Device class
- Class 2
- Regulation
- 21 CFR 886.4790
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shanghai, CN
Recent devices under product code HOZ
view allMore clearances from Huizhou Foryou Medical Devices Co., Ltd.
view all- K254256 — LUOFUCON® Wound Matrix
- K250642 — LUOFUCON® Skin and Wound Cleanser (Spray, Mist, Squeeze, Bottle.)
- K240809 — LUOFUCON® Silver Collagen Dressing
- K242856 — LUOFUCON® Silicone Ag+ Foam Dressing (Prescription use)/ LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing (OTC use) (Bordered, Bordered Lite, Non-Bordered, and Transfer)
- K240485 — LUOFUCON® Extra Silver Gelling Fiber Dressing Plus (Prescription use),LUOFUCON® Silver Antimicrobial Gelling Fiber Dressing Plus (OTC use)
Data sourced from openFDA. This site is unofficial and independent of the FDA.