SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11— 510(k) K850883
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K850883 for SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11, Substantially Equivalent on 1985-03-20. Applicant: Storz Instrument Co.. Device class: 2.
Clearance details
- Applicant
- Storz Instrument Co.
- 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
- St. Louis, MO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.