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FDA 510(k)

CARERITE & COST RITE NYLON STERILIZATION FILM

K-Number: K870147 · 1987-04-23

ApplicantCost Rite Health Products, Inc.
Decision Date1987-04-23
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARERITE & COST RITE NYLON STERILIZATION FILM is the device name listed in this FDA 510(k) record. The listed applicant is Cost Rite Health Products, Inc.. It received FDA 510(k) clearance on 1987-04-23 under 510(k) number K870147. 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 CARERITE & COST RITE NYLON STERILIZATION FILM?

CARERITE & COST RITE NYLON STERILIZATION FILM is a medical device that received FDA 510(k) clearance on 1987-04-23. The listed applicant is Cost Rite Health Products, Inc.. The 510(k) number is K870147.

When did CARERITE & COST RITE NYLON STERILIZATION FILM receive FDA 510(k) clearance?

CARERITE & COST RITE NYLON STERILIZATION FILM received FDA 510(k) clearance on 1987-04-23, under 510(k) number K870147.

Who is the listed applicant for CARERITE & COST RITE NYLON STERILIZATION FILM?

The FDA 510(k) record lists Cost Rite Health Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARERITE & COST RITE NYLON STERILIZATION FILM?

The FDA product code for CARERITE & COST RITE NYLON STERILIZATION FILM is FRG.

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Other records listing Cost Rite Health Products, 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.

K891141CARERITE FACE MASKK890667RUBBER DAMK873705CARERITE FACE MASKK871798FILM AND PAPER COMBINATION STERILIZING BAGK871736CARERITE BIOPACK GINGIVAL RETRACTION CORDK870906CARERITE INTERDENTAL BRUSHES, MODELS 3500 & 4500

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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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