KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET— 510(k) K970969
Substantially EquivalentThe Kendal Co.
FDA 510(k) clearance K970969 for KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET, Substantially Equivalent on 1997-04-23. Applicant: The Kendal Co.. Device class: 2.
Clearance details
- Applicant
- The Kendal Co.
- Product code
- Code KOB
- Device class
- Class 2
- Regulation
- 21 CFR 876.5090
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mansfield, MA, US
Recent devices under product code KOB
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view all- K000087 — MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
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- K991758 — MONOJECT INSULIN SYRINGE
- K951488 — KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
- K942664 — KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.