SCLERAL BUCKLING IMPLANTS DIF/TYPES— 510(k) K832481
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K832481 for SCLERAL BUCKLING IMPLANTS DIF/TYPES, Substantially Equivalent on 1983-09-20. Applicant: Storz Instrument Co.. Device class: 2.
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code HQX
- Device class
- Class 2
- Regulation
- 21 CFR 886.3340
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code HQX
view all- K023481 — MICROVISION SCLERAL BUCKLING COMPONENTS
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- K963219 — RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES
- K950806 — SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
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Data sourced from openFDA. This site is unofficial and independent of the FDA.