ANEROID SPHYGMOMETER
K-Number: K771501 · 1977-08-30
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Device Summary
Frequently Asked Questions
What is the ANEROID SPHYGMOMETER?
ANEROID SPHYGMOMETER is a medical device that received FDA 510(k) clearance on 1977-08-30. The listed applicant is Swartz Medical Equipment. The 510(k) number is K771501.
When did ANEROID SPHYGMOMETER receive FDA 510(k) clearance?
ANEROID SPHYGMOMETER received FDA 510(k) clearance on 1977-08-30, under 510(k) number K771501.
Who is the listed applicant for ANEROID SPHYGMOMETER?
The FDA 510(k) record lists Swartz Medical Equipment as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANEROID SPHYGMOMETER?
The FDA product code for ANEROID SPHYGMOMETER 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 Swartz Medical Equipment 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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