OLYMPUS PR-23Q DISPOSABLE CANNULA (BALL TIP)— 510(k) K950729
Substantially EquivalentOlympus America, Inc.
FDA 510(k) clearance K950729 for OLYMPUS PR-23Q DISPOSABLE CANNULA (BALL TIP), Substantially Equivalent on 1995-03-17. Applicant: Olympus America, Inc.. Device class: 2.
Clearance details
- Applicant
- Olympus America, Inc.
- Product code
- Code ODD
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
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More clearances from Olympus America, Inc.
view allRecalls naming K950729
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K950729.
Data sourced from openFDA. This site is unofficial and independent of the FDA.