Tray, Blood Gas, Cat. No. 4010

FDA 510(k) K770361 · Concord Laboratories, Inc.

Substantially Equivalent

510(k) numberK770361

Submission

Device name
Tray, Blood Gas, Cat. No. 4010
Applicant
Concord Laboratories, Inc.
Mchenry, IL, US
Received
February 22, 1977
Decision date
April 5, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

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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
K862039Concord Care Tray · Traditional 07/03/1986SESD
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

Questions and answers

When was Tray, Blood Gas, Cat. No. 4010 cleared by the FDA?

Tray, Blood Gas, Cat. No. 4010 (K770361) received a 510(k) decision of Substantially Equivalent on April 5, 1977, 42 days after the submission was received.

What is the product code of K770361?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.