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FDA 510(k)

RX TEXTILES STERILE STOCKINETTE

K-Number: K960803 · 1996-07-12

Decision Date1996-07-12
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RX TEXTILES STERILE STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Rx Textiles, Inc.. It received FDA 510(k) clearance on 1996-07-12 under 510(k) number K960803. 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 RX TEXTILES STERILE STOCKINETTE?

RX TEXTILES STERILE STOCKINETTE is a medical device that received FDA 510(k) clearance on 1996-07-12. The listed applicant is Rx Textiles, Inc.. The 510(k) number is K960803.

When did RX TEXTILES STERILE STOCKINETTE receive FDA 510(k) clearance?

RX TEXTILES STERILE STOCKINETTE received FDA 510(k) clearance on 1996-07-12, under 510(k) number K960803.

Who is the listed applicant for RX TEXTILES STERILE STOCKINETTE?

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

What is the FDA product code for RX TEXTILES STERILE STOCKINETTE?

The FDA product code for RX TEXTILES STERILE STOCKINETTE 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.

Related Devices (Code: KKX)

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.

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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