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FDA 510(k)

GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES

K-Number: K052665 · 2006-02-27

ApplicantGranton Medical , Ltd.
Decision Date2006-02-27
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES is the device name listed in this FDA 510(k) record. The listed applicant is Granton Medical , Ltd.. It received FDA 510(k) clearance on 2006-02-27 under 510(k) number K052665. 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 GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES?

GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES is a medical device that received FDA 510(k) clearance on 2006-02-27. The listed applicant is Granton Medical , Ltd.. The 510(k) number is K052665.

When did GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES receive FDA 510(k) clearance?

GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES received FDA 510(k) clearance on 2006-02-27, under 510(k) number K052665.

Who is the listed applicant for GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES?

The FDA 510(k) record lists Granton Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES?

The FDA product code for GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES is FRG.

Related Clinical Trials

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Other records listing Granton Medical , Ltd. 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.

K023025SELF SEAL STERILIZATION POUCH

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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