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FDA 510(k)

Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap

K-Number: K171533 · 2017-06-29

ApplicantAhlstrom Nonwovens, LLC
Decision Date2017-06-29
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Ahlstrom Nonwovens, LLC. It received FDA 510(k) clearance on 2017-06-29 under 510(k) number K171533. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?

Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2017-06-29. The listed applicant is Ahlstrom Nonwovens, LLC. The 510(k) number is K171533.

When did Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap receive FDA 510(k) clearance?

Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap received FDA 510(k) clearance on 2017-06-29, under 510(k) number K171533.

Who is the listed applicant for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?

The FDA 510(k) record lists Ahlstrom Nonwovens, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?

The FDA product code for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap is FRG.

Other records listing Ahlstrom Nonwovens, LLC 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.

K160755Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap

Related Devices (Code: FRG)

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.

K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* HEAVY-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* STANDARD-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* H300W Sterilization Wrap with ASSURE-DRY* TechnologyO&M Halyard, Inc.K252823Dukal Crepe Paper Sterilization WrapDukal, LLCK253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap; HALYARD* SEQUENTIAL Sterilization Wrap; HALYARD* SMART-FOLD* Sterilization WrapO&M Halyard, Inc.K251347Sterilization Pouch/RollSterivic Medical Co., Ltd.K251177Self-Seal Sterilization Pouch and RollGuangdong Maidi Medical Co., Ltd.K250306Chex-All Sterilization Pouches and TubesPropper Manufacturing Co., Inc.

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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