FDA 510(k)

ABSORBENT, FIBER, OPERATING ROOM TOWELS

K-Number: K860936 · 1986-04-04

Decision Date1986-04-04

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ABSORBENT, FIBER, OPERATING ROOM TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 1986-04-04 under 510(k) number K860936. 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 ABSORBENT, FIBER, OPERATING ROOM TOWELS?

ABSORBENT, FIBER, OPERATING ROOM TOWELS is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K860936.

When did ABSORBENT, FIBER, OPERATING ROOM TOWELS receive FDA 510(k) clearance?

ABSORBENT, FIBER, OPERATING ROOM TOWELS received FDA 510(k) clearance on 1986-04-04, under 510(k) number K860936.

Who is the listed applicant for ABSORBENT, FIBER, OPERATING ROOM TOWELS?

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

What is the FDA product code for ABSORBENT, FIBER, OPERATING ROOM TOWELS?

The FDA product code for ABSORBENT, FIBER, OPERATING ROOM TOWELS is KKX.

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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.