NEUROSPONGES
K-Number: K812391 · 1981-11-24
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Device Summary
Frequently Asked Questions
What is the NEUROSPONGES?
NEUROSPONGES is a medical device that received FDA 510(k) clearance on 1981-11-24. The listed applicant is Winn Hirsch & Assoc.. The 510(k) number is K812391.
When did NEUROSPONGES receive FDA 510(k) clearance?
NEUROSPONGES received FDA 510(k) clearance on 1981-11-24, under 510(k) number K812391.
Who is the listed applicant for NEUROSPONGES?
The FDA 510(k) record lists Winn Hirsch & Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROSPONGES?
The FDA product code for NEUROSPONGES is GDY.
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 Winn Hirsch & Assoc. 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: GDY)
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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