FDA 510(k)

OPERATING ROOM TOWELS - STERILE/NON STERILE

K-Number: K863871 · 1986-10-24

Decision Date1986-10-24

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

OPERATING ROOM TOWELS - STERILE/NON STERILE 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 K863871. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING ROOM TOWELS - STERILE/NON STERILE?

OPERATING ROOM TOWELS - STERILE/NON STERILE 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 K863871.

When did OPERATING ROOM TOWELS - STERILE/NON STERILE receive FDA 510(k) clearance?

OPERATING ROOM TOWELS - STERILE/NON STERILE received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863871.

Who is the listed applicant for OPERATING ROOM TOWELS - STERILE/NON STERILE?

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 OPERATING ROOM TOWELS - STERILE/NON STERILE?

The FDA product code for OPERATING ROOM TOWELS - STERILE/NON STERILE is KKX.

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.

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Other records listing Med-Tex, Inc. as applicant

K885099MULTIPLE (STERILE SURGICAL TOWELS)K863870GAUZE, NONABSORBABLE, NON-MEDICATED (INTERNAL)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.