ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES
K-Number: K935429 · 1994-11-01
Advertisement
Device Summary
Frequently Asked Questions
What is the ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES?
ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Arbo Medical, Inc.. The 510(k) number is K935429.
When did ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES receive FDA 510(k) clearance?
ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES received FDA 510(k) clearance on 1994-11-01, under 510(k) number K935429.
Who is the listed applicant for ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES?
The FDA 510(k) record lists Arbo Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES?
The FDA product code for ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES is DRX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Arbo Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DRX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement