ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES
K-Number: K935437 · 1995-04-06
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Device Summary
Frequently Asked Questions
What is the ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES?
ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES is a medical device that received FDA 510(k) clearance on 1995-04-06. The listed applicant is Arbo Medical, Inc.. The 510(k) number is K935437.
When did ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES receive FDA 510(k) clearance?
ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES received FDA 510(k) clearance on 1995-04-06, under 510(k) number K935437.
Who is the listed applicant for ARBO H85V/H87V/H27V DISPOS MONIT 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 H85V/H87V/H27V DISPOS MONIT ELECTRODES?
The FDA product code for ARBO H85V/H87V/H27V DISPOS MONIT 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.
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