Curity Plastic Loss of Resistance Syringe
K922162 is the FDA 510(k) clearance record for CURITY PLASTIC LOSS OF RESISTANCE SYRINGE, a class II device, cleared for Kendall Healthcare Products Co. Div.Of Tyco Health on under FDA product code CAZ (Anesthesia Conduction Kit). FDA's definition for product code CAZ reads: "This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the...". FDA records list 66 510(k) clearances for Kendall Healthcare Products Co. Div.Of Tyco Health, from to . As of , FDA records show no recalls naming K922162.
Clearance record
- Decision date
- Received
- (335 days to decision)
- Product code
- CAZ Anesthesia Conduction Kit
- Regulation
- 21 CFR 868.5140
- Device class
- Class II
- Review panel
- Anesthesiology
- Applicant
- Kendall Healthcare Products Co. Div.Of Tyco Health 15 Hampshire St., Mansfield MA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code CAZ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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