Concord Care Tray

FDA 510(k) K862039 · Concord Laboratories, Inc.

Unknown

510(k) numberK862039

Submission

Device name
Concord Care Tray
Applicant
Concord Laboratories, Inc.
Keene, NH, US
Received
May 28, 1986
Decision date
July 3, 1986
Decision
Unknown (SESD)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Concord Laboratories, Inc.

510(k)DeviceDecision
K883840Dri-Vent Arterial Blood Sampling KitLKB · Traditional 05/16/1989SESD
K871825Meconium Suction CatheterBSY · Traditional 06/29/1987SE
K864535Tracheobronchial Suction Catheter, Cat. No. 6110BSY · Traditional 01/06/1987SE
K854601Spring Guide Catheter Anesthesia Conduction CathBSO · Traditional 01/10/1986SE
K854327Subcutaneous Tunneling Needles & HandlesGCB · Traditional 11/13/1985SE
K851134Regional Anesthesia TraysCAZ · Traditional 07/15/1985SESD
K842095Epidural TraysCAZ · Traditional 07/03/1984SE
K841486Arterial Blood Sampling KitsCBT · Traditional 05/23/1984SE
K840987Vaporized HeparinCBT · Traditional 04/05/1984SE
K840986Prefilled Pulsator SyringeCBT · Traditional 04/05/1984SE

Questions and answers

When was Concord Care Tray cleared by the FDA?

Concord Care Tray (K862039) received a 510(k) decision of Unknown on July 3, 1986, 36 days after the submission was received.