510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062999Substantially Equivalent

Opticath Central Venous Oximetry Probe with Seal with Heparin

Abbott Medical, Lake Forest IL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062999 is the FDA 510(k) clearance record for OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN, a class II device, cleared for Hospira, Inc. on under FDA product code DQE (Catheter, Oximeter, Fiber-Optic). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K062999.

Clearance record

Decision date
Received
(32 days to decision)
Product code
DQE Catheter, Oximeter, Fiber-Optic
Regulation
21 CFR 870.1230
Device class
Class II
Review panel
Cardiovascular
Applicant
Hospira, Inc. 275 N. Field Dr., Lake Forest IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQE

Trailing 12 months

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

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