ANTACHE ANTI-HEADACHE DEVICE
K-Number: K834111 · 1984-02-03
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Device Summary
Frequently Asked Questions
What is the ANTACHE ANTI-HEADACHE DEVICE?
ANTACHE ANTI-HEADACHE DEVICE is a medical device that received FDA 510(k) clearance on 1984-02-03. The listed applicant is Bio Sig Instruments, Inc.. The 510(k) number is K834111.
When did ANTACHE ANTI-HEADACHE DEVICE receive FDA 510(k) clearance?
ANTACHE ANTI-HEADACHE DEVICE received FDA 510(k) clearance on 1984-02-03, under 510(k) number K834111.
Who is the listed applicant for ANTACHE ANTI-HEADACHE DEVICE?
The FDA 510(k) record lists Bio Sig Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANTACHE ANTI-HEADACHE DEVICE?
The FDA product code for ANTACHE ANTI-HEADACHE DEVICE 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 Bio Sig Instruments, 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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