ZEE SPHYGMOMANOMETER
K-Number: K823501 · 1983-01-21
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Device Summary
Frequently Asked Questions
What is the ZEE SPHYGMOMANOMETER?
ZEE SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Zee Medical Products Co., Inc.. The 510(k) number is K823501.
When did ZEE SPHYGMOMANOMETER receive FDA 510(k) clearance?
ZEE SPHYGMOMANOMETER received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823501.
Who is the listed applicant for ZEE SPHYGMOMANOMETER?
The FDA 510(k) record lists Zee Medical Products Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZEE SPHYGMOMANOMETER?
The FDA product code for ZEE SPHYGMOMANOMETER 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 Zee Medical Products Co., 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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