Model 110-5 & 140-8

FDA 510(k) K842005 · Camino Laboratories, Inc.

Substantially Equivalent

510(k) numberK842005

Submission

Device name
Model 110-5 & 140-8
Applicant
Camino Laboratories, Inc.
Walker, MI, US
Received
May 17, 1984
Decision date
August 3, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXO – Transducer, Pressure, Catheter Tip
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2870
Specialty
Cardiovascular

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More from Edwards Lifeciences, LLC

510(k)DeviceDecision
K932769Camino Ventricular Drainage SystemJXG · Traditional 03/30/1995SE
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K920088Camino Ventricular NeedleHCD · Traditional 05/01/1992SE
K914735Ventricular Pressure Monitoring Kit, Model 110-4HMGWM · Traditional 01/17/1992SE
K912833Camino Model M420: Monit Inter W/Mean Pres DisplayDSK · Traditional 09/23/1991SE
K893232Model V420 Direct Pressure Monitor & 427 WaveformDSK · Traditional 07/14/1989SE
K881183Ventricular Bolt Pressure Monitoring Kit #110-4HGWM · Traditional 05/04/1988SE
K863969Camino Compartmental Press Monitor CATH/110-4DDXO · Traditional 05/27/1987SE
K861961Camino CSF Drainage System Model 040JXG · Traditional 08/12/1986SE

Questions and answers

When was Model 110-5 & 140-8 cleared by the FDA?

Model 110-5 & 140-8 (K842005) received a 510(k) decision of Substantially Equivalent on August 3, 1984, 78 days after the submission was received.

What is the product code of K842005?

The FDA product code is DXO – Transducer, Pressure, Catheter Tip, a Class II (moderate risk) device regulated under 21 CFR 870.2870.