NEURO-SORB PATTIES
K-Number: K770894 · 1977-06-20
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Device Summary
Frequently Asked Questions
What is the NEURO-SORB PATTIES?
NEURO-SORB PATTIES is a medical device that received FDA 510(k) clearance on 1977-06-20. The listed applicant is Instranetics, Inc.. The 510(k) number is K770894.
When did NEURO-SORB PATTIES receive FDA 510(k) clearance?
NEURO-SORB PATTIES received FDA 510(k) clearance on 1977-06-20, under 510(k) number K770894.
Who is the listed applicant for NEURO-SORB PATTIES?
The FDA 510(k) record lists Instranetics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEURO-SORB PATTIES?
The FDA product code for NEURO-SORB PATTIES is HBA.
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 Instranetics, 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: HBA)
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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