510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K981035Substantially Equivalent

Pro-Vent, Pulsator Arterial Blood Sampling Syringes

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

K981035 is the FDA 510(k) clearance record for PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES, a class II device, cleared for Sims Portex, Inc. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show one recall naming K981035.

Clearance record

Decision date
Received
(33 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sims Portex, Inc. 10 Bowman Dr., Keene NH
510(k) summary
Summary
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260