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FDA 510(k)

INFECTION CONTROL TOWEL

K-Number: K822484 · 1982-09-30

ApplicantAmerican Threshold Industries, Inc.
Decision Date1982-09-30
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFECTION CONTROL 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 1982-09-30 under 510(k) number K822484. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFECTION CONTROL TOWEL?

INFECTION CONTROL TOWEL is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is American Threshold Industries, Inc.. The 510(k) number is K822484.

When did INFECTION CONTROL TOWEL receive FDA 510(k) clearance?

INFECTION CONTROL TOWEL received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822484.

Who is the listed applicant for INFECTION CONTROL 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 INFECTION CONTROL TOWEL?

The FDA product code for INFECTION CONTROL TOWEL is LDQ.

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Other records listing American Threshold Industries, 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.

K971483SECURE-WRAP (TM) STERILIZATION WRAPK953878BOUFFANT CAPK953879SURGEON'S CAPK952115BARRIER GOWN, KOOL-GARD BACKLESS GOWNK952114KOOL GARD SINGLES GOWNK952116COVER GOWN

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Related Devices (Code: LDQ)

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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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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