510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K933711Unknown

E-Sp Combined Epidural-Spinal Anesthesia Tray

Neurodelivery Technology, Inc., Labanon NH / Traditional, Unknown
FDA source (opens on fda.gov)

K933711 is the FDA 510(k) clearance record for E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY, a class II device, cleared for Neurodelivery Technology, Inc. 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 3 510(k) clearances for Neurodelivery Technology, Inc., from to . As of , FDA records show no recalls naming K933711.

Clearance record

Decision date
Received
(115 days to decision)
Product code
CAZ Anesthesia Conduction Kit
Regulation
21 CFR 868.5140
Device class
Class II
Review panel
Anesthesiology
Applicant
Neurodelivery Technology, Inc. Chiron Springs Offices, Labanon NH
510(k) summary
Statement
Third party review
No

Clearances, product code CAZ

Trailing 12 months
1 clearance under product code CAZ in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260