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FDA 510(k)

DISPOSABLE O.R. TOWEL

K-Number: K912110 · 1991-07-25

ApplicantAmerican Threshold Industries, Inc.
Decision Date1991-07-25
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE O.R. TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is American Threshold Industries, Inc.. It received FDA 510(k) clearance on 1991-07-25 under 510(k) number K912110. 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 DISPOSABLE O.R. TOWEL?

DISPOSABLE O.R. TOWEL is a medical device that received FDA 510(k) clearance on 1991-07-25. The listed applicant is American Threshold Industries, Inc.. The 510(k) number is K912110.

When did DISPOSABLE O.R. TOWEL receive FDA 510(k) clearance?

DISPOSABLE O.R. TOWEL received FDA 510(k) clearance on 1991-07-25, under 510(k) number K912110.

Who is the listed applicant for DISPOSABLE O.R. TOWEL?

The FDA 510(k) record lists American Threshold Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE O.R. TOWEL?

The FDA product code for DISPOSABLE O.R. TOWEL is KKX.

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Other records listing American Threshold Industries, Inc. as applicant

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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.

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