SOMATOSENSORY STIMULUS SYSTEM
K-Number: K913604 · 1991-12-09
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Device Summary
Frequently Asked Questions
What is the SOMATOSENSORY STIMULUS SYSTEM?
SOMATOSENSORY STIMULUS SYSTEM is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K913604.
When did SOMATOSENSORY STIMULUS SYSTEM receive FDA 510(k) clearance?
SOMATOSENSORY STIMULUS SYSTEM received FDA 510(k) clearance on 1991-12-09, under 510(k) number K913604.
Who is the listed applicant for SOMATOSENSORY STIMULUS SYSTEM?
The FDA 510(k) record lists Biomagnetic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOMATOSENSORY STIMULUS SYSTEM?
The FDA product code for SOMATOSENSORY STIMULUS SYSTEM is GZP.
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 Biomagnetic Technologies, 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: GZP)
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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