CLINICAL EMG MODEL 133
K-Number: K771577 · 1977-08-26
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Device Summary
Frequently Asked Questions
What is the CLINICAL EMG MODEL 133?
CLINICAL EMG MODEL 133 is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Calnor of EL Paseo, Inc.. The 510(k) number is K771577.
When did CLINICAL EMG MODEL 133 receive FDA 510(k) clearance?
CLINICAL EMG MODEL 133 received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771577.
Who is the listed applicant for CLINICAL EMG MODEL 133?
The FDA 510(k) record lists Calnor of EL Paseo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINICAL EMG MODEL 133?
The FDA product code for CLINICAL EMG MODEL 133 is HCC.
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 Calnor of EL Paseo, 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: HCC)
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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