OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C
K-Number: K903134 · 1991-01-08
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Device Summary
Frequently Asked Questions
What is the OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C?
OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C is a medical device that received FDA 510(k) clearance on 1991-01-08. The listed applicant is Omron Marshall Products, Inc.. The 510(k) number is K903134.
When did OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C receive FDA 510(k) clearance?
OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C received FDA 510(k) clearance on 1991-01-08, under 510(k) number K903134.
Who is the listed applicant for OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C?
The FDA 510(k) record lists Omron Marshall Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C?
The FDA product code for OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C is DXN.
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 Omron Marshall Products, 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: DXN)
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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