CONPHAR CHECKMATE SPHYGMOMANOMETER
K-Number: K801187 · 1980-06-09
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Device Summary
Frequently Asked Questions
What is the CONPHAR CHECKMATE SPHYGMOMANOMETER?
CONPHAR CHECKMATE SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1980-06-09. The listed applicant is Conphar, Inc.. The 510(k) number is K801187.
When did CONPHAR CHECKMATE SPHYGMOMANOMETER receive FDA 510(k) clearance?
CONPHAR CHECKMATE SPHYGMOMANOMETER received FDA 510(k) clearance on 1980-06-09, under 510(k) number K801187.
Who is the listed applicant for CONPHAR CHECKMATE SPHYGMOMANOMETER?
The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONPHAR CHECKMATE SPHYGMOMANOMETER?
The FDA product code for CONPHAR CHECKMATE 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 Conphar, 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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