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FDA 510(k)

NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION

K-Number: K951704 · 1995-06-28

ApplicantProducts For Medicine
Decision Date1995-06-28
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION is the device name listed in this FDA 510(k) record. The listed applicant is Products For Medicine. It received FDA 510(k) clearance on 1995-06-28 under 510(k) number K951704. 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 NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION?

NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION is a medical device that received FDA 510(k) clearance on 1995-06-28. The listed applicant is Products For Medicine. The 510(k) number is K951704.

When did NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION receive FDA 510(k) clearance?

NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION received FDA 510(k) clearance on 1995-06-28, under 510(k) number K951704.

Who is the listed applicant for NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION?

The FDA 510(k) record lists Products For Medicine as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION?

The FDA product code for NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATION is FRG.

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Other records listing Products For Medicine 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.

K963227WHITE SUN LIGHT SOURCE MODEL #: XL300 AND #: XL175K955510X6000D SILENT SUN LIGHT SOURCEK953089I-SPOUSEK951703TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORSK883658I-SPOSE EYE SHIELD

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

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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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