Electrophysiology Electrode Cath. W/Silver/Silver

FDA 510(k) K881966 · C.R. Bard, Inc.

Substantially Equivalent

510(k) numberK881966

Submission

Device name
Electrophysiology Electrode Cath. W/Silver/Silver
Applicant
C.R. Bard, Inc.
Billerica, MA, US
Received
May 11, 1988
Decision date
October 4, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DRF – Catheter, Electrode Recording, Or Probe, Electrode Recording
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1220
Specialty
Cardiovascular

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Questions and answers

When was Electrophysiology Electrode Cath. W/Silver/Silver cleared by the FDA?

Electrophysiology Electrode Cath. W/Silver/Silver (K881966) received a 510(k) decision of Substantially Equivalent on October 4, 1988, 146 days after the submission was received.

What is the product code of K881966?

The FDA product code is DRF – Catheter, Electrode Recording, Or Probe, Electrode Recording, a Class II (moderate risk) device regulated under 21 CFR 870.1220.