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FDA 510(k)

INDUS TEXTILES TOWEL-STERILE AND NON-STERILE

K-Number: K013958 · 2002-08-19

ApplicantIndus Textiles, Inc.
Decision Date2002-08-19
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INDUS TEXTILES TOWEL-STERILE AND NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Indus Textiles, Inc.. It received FDA 510(k) clearance on 2002-08-19 under 510(k) number K013958. 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 INDUS TEXTILES TOWEL-STERILE AND NON-STERILE?

INDUS TEXTILES TOWEL-STERILE AND NON-STERILE is a medical device that received FDA 510(k) clearance on 2002-08-19. The listed applicant is Indus Textiles, Inc.. The 510(k) number is K013958.

When did INDUS TEXTILES TOWEL-STERILE AND NON-STERILE receive FDA 510(k) clearance?

INDUS TEXTILES TOWEL-STERILE AND NON-STERILE received FDA 510(k) clearance on 2002-08-19, under 510(k) number K013958.

Who is the listed applicant for INDUS TEXTILES TOWEL-STERILE AND NON-STERILE?

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

What is the FDA product code for INDUS TEXTILES TOWEL-STERILE AND NON-STERILE?

The FDA product code for INDUS TEXTILES TOWEL-STERILE AND NON-STERILE is KKX.

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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.

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