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Capiox Cardioplegia

by Terumo Medical Corp.

510(k) K982467

Capiox Cardioplegia is a medical device (FDA Class II; FDA product code DTR, Heat-Exchanger, Cardiopulmonary Bypass) made by Terumo Medical Corp., cleared under FDA 510(k) K982467 on 23 Jun 1999, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK982467 Date23 Jun 1999ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
DTR
Device class
Class II
Regulation
21 CFR Part 870.4240
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code DTR (Heat-Exchanger, Cardiopulmonary Bypass).

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