MODEL HBP-1300
K-Number: K113185 · 2012-01-27
Advertisement
Device Summary
Frequently Asked Questions
What is the MODEL HBP-1300?
MODEL HBP-1300 is a medical device that received FDA 510(k) clearance on 2012-01-27. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K113185.
When did MODEL HBP-1300 receive FDA 510(k) clearance?
MODEL HBP-1300 received FDA 510(k) clearance on 2012-01-27, under 510(k) number K113185.
Who is the listed applicant for MODEL HBP-1300?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL HBP-1300?
The FDA product code for MODEL HBP-1300 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 Healthcare, 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.
Advertisement