510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832396Substantially Equivalent

Central Venous Access Catheter Cvac

Gish Biomedical, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832396 is the FDA 510(k) clearance record for CENTRAL VENOUS ACCESS CATHETER CVAC, a class II device, cleared for Gish Biomedical, Inc. on under FDA product code DOY (Radioimmunoassay, Digoxin (3-H), Goat Antibody, 2nd Antibody Sep.). FDA records list 75 510(k) clearances for Gish Biomedical, Inc., from to . As of , FDA records show no recalls naming K832396.

Clearance record

Decision date
Received
(42 days to decision)
Product code
DOY Radioimmunoassay, Digoxin (3-H), Goat Antibody, 2nd Antibody Sep.
Regulation
21 CFR 862.3320
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Gish Biomedical, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DOY

Trailing 12 months

FDA records hold no clearances under product code DOY in the trailing twelve months.

FDA records show no clearances under product code DOY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DOY, 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 20260
October 20260