DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883
K-Number: K951977 · 1995-10-24
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Device Summary
Frequently Asked Questions
What is the DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883?
DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883 is a medical device that received FDA 510(k) clearance on 1995-10-24. The listed applicant is Integrated Display Technology, Ltd.. The 510(k) number is K951977.
When did DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883 receive FDA 510(k) clearance?
DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883 received FDA 510(k) clearance on 1995-10-24, under 510(k) number K951977.
Who is the listed applicant for DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883?
The FDA 510(k) record lists Integrated Display Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883?
The FDA product code for DIGITAL BLOOD PRESSURE METER - MODEL NO.: BPM883 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 Integrated Display Technology, Ltd. 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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