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)

GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL)

K-Number: K863870 · 1986-10-24

ApplicantMed-Tex, Inc.
Decision Date1986-10-24
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL) is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tex, Inc.. It received FDA 510(k) clearance on 1986-10-24 under 510(k) number K863870. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL)?

GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL) is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Med-Tex, Inc.. The 510(k) number is K863870.

When did GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL) receive FDA 510(k) clearance?

GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL) received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863870.

Who is the listed applicant for GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL)?

The FDA 510(k) record lists Med-Tex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL)?

The FDA product code for GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL) 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 Med-Tex, 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: 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.

↑