STORZ ENT/OPHTHALMIC MAXI CHAIR— 510(k) K870112
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K870112 for STORZ ENT/OPHTHALMIC MAXI CHAIR, Substantially Equivalent on 1987-02-12. Applicant: Storz Instrument Co.. Device class: 1.
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code HME
- Device class
- Class 1
- Regulation
- 21 CFR 886.1140
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Recent devices under product code HME
view allMore clearances from Storz Instrument Co.
view all- K980100 — STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACK
- K980488 — STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM
- K972664 — STORZ MILLENNIUM VISCOUS FLUID SYSTEM
- K971439 — STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLES
- K964743 — STORZ E8010 ERGOTEC/PREMIERE ADAPTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.