STSTORZ DP5300 AND DP9502 STERILE DRAPES— 510(k) K934445
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K934445 for STSTORZ DP5300 AND DP9502 STERILE DRAPES, Substantially Equivalent on 1994-04-11. Applicant: Storz Instrument Co.. Device class: 2.
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code KKX
- Device class
- Class 2
- Regulation
- 21 CFR 878.4370
- Advisory panel
- General, Plastic Surgery
- 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.