Q-5000— 510(k) K961971
Substantially EquivalentStryker Endoscopy
FDA 510(k) clearance K961971 for Q-5000, Substantially Equivalent on 1996-06-28. Applicant: Stryker Endoscopy. Device class: 2.
Clearance details
- Applicant
- Stryker Endoscopy
- Product code
- Code FSS
- Device class
- Class 2
- Regulation
- 21 CFR 878.4580
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
Recent devices under product code FSS
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- K984124 — AESCULAP XENON LIGHT SOURCE
- K981962 — CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE
- K981821 — VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR
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Data sourced from openFDA. This site is unofficial and independent of the FDA.