PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP
K-Number: K860634 · 1986-07-01
Advertisement
Device Summary
Frequently Asked Questions
What is the PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP?
PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP is a medical device that received FDA 510(k) clearance on 1986-07-01. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K860634.
When did PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP receive FDA 510(k) clearance?
PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP received FDA 510(k) clearance on 1986-07-01, under 510(k) number K860634.
Who is the listed applicant for PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP?
The FDA 510(k) record lists Panasonic Co. Div. Matsu Elec. Corp. America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP?
The FDA product code for PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP 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 Panasonic Co. Div. Matsu Elec. Corp. America 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