510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K893766Substantially Equivalent

Lifecare Cont. Epidural Cath. for Morphine Sulfate

Abbott Medical, Abbott Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893766 is the FDA 510(k) clearance record for LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE, a class II device, cleared for Abbott Laboratories on under FDA product code MAJ (Catheter, Percutaneous, Intraspinal, Short Term). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K893766.

Clearance record

Decision date
Received
(166 days to decision)
Product code
MAJ Catheter, Percutaneous, Intraspinal, Short Term
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Abbott Laboratories One Abbott Park Rd., Abbott Park IL
Third party review
No

Clearances, product code MAJ

Trailing 12 months

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

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