Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NEUROLOGICAL SPONGES (PATTIES)

K-Number: K791871 · 1979-11-05

ApplicantCarwild Corp.
Decision Date1979-11-05
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

NEUROLOGICAL SPONGES (PATTIES) is the device name listed in this FDA 510(k) record. The listed applicant is Carwild Corp.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K791871. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROLOGICAL SPONGES (PATTIES)?

NEUROLOGICAL SPONGES (PATTIES) is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Carwild Corp.. The 510(k) number is K791871.

When did NEUROLOGICAL SPONGES (PATTIES) receive FDA 510(k) clearance?

NEUROLOGICAL SPONGES (PATTIES) received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791871.

Who is the listed applicant for NEUROLOGICAL SPONGES (PATTIES)?

The FDA 510(k) record lists Carwild Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROLOGICAL SPONGES (PATTIES)?

The FDA product code for NEUROLOGICAL SPONGES (PATTIES) is EFQ.

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 Carwild 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: EFQ)

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.

↑