510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K110053Substantially Equivalent

Correctinject Safety System, Catheter Connector, Filter, Infusion Adaptor, Syringe Kit

Abbott Medical, Keene NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110053 is the FDA 510(k) clearance record for CORRECTINJECT SAFETY SYSTEM, CATHETER CONNECTOR, FILTER, INFUSION ADAPTOR, SYRINGE KIT, a class II device, cleared for Smiths Medical Asd, 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 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K110053.

Clearance record

Decision date
Received
(616 days to decision)
Product code
CAZ Anesthesia Conduction Kit
Regulation
21 CFR 868.5140
Device class
Class II
Review panel
Anesthesiology
Applicant
Smiths Medical Asd, Inc. 10 Bowman Dr., Keene NH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CAZ

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