STORZ E9050 & E9055 DIAMOND KNIVES— 510(k) K861732
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K861732 for STORZ E9050 & E9055 DIAMOND KNIVES, Substantially Equivalent on 1986-05-28. Applicant: Storz Instrument Co.. Device class: 1.
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code HNN
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
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Adverse events under product code HNN
product code HNN- Injury
- 183
- Malfunction
- 4,106
- Total
- 4,289
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.