CONPHAR PALM ANEROID SPHYGMOMANOMETER
K-Number: K813302 · 1982-01-22
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Device Summary
Frequently Asked Questions
What is the CONPHAR PALM ANEROID SPHYGMOMANOMETER?
CONPHAR PALM ANEROID SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Conphar, Inc.. The 510(k) number is K813302.
When did CONPHAR PALM ANEROID SPHYGMOMANOMETER receive FDA 510(k) clearance?
CONPHAR PALM ANEROID SPHYGMOMANOMETER received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813302.
Who is the listed applicant for CONPHAR PALM ANEROID 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 PALM ANEROID SPHYGMOMANOMETER?
The FDA product code for CONPHAR PALM ANEROID SPHYGMOMANOMETER is DXQ.
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: DXQ)
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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