SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.
K-Number: K871964 · 1987-10-01
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Device Summary
Frequently Asked Questions
What is the SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.?
SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. is a medical device that received FDA 510(k) clearance on 1987-10-01. The listed applicant is Siegen Corp.. The 510(k) number is K871964.
When did SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. receive FDA 510(k) clearance?
SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. received FDA 510(k) clearance on 1987-10-01, under 510(k) number K871964.
Who is the listed applicant for SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.?
The FDA 510(k) record lists Siegen Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.?
The FDA product code for SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. is GWF.
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 Siegen Corp. 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: GWF)
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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