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FDA 510(k)

STERILIZER WRAP (CAT#221831,2,3,4,5,6)

K-Number: K760661 · 1976-12-02

ApplicantC.R. Bard, Inc.
Decision Date1976-12-02
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZER WRAP (CAT#221831,2,3,4,5,6) is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K760661. 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 STERILIZER WRAP (CAT#221831,2,3,4,5,6)?

STERILIZER WRAP (CAT#221831,2,3,4,5,6) is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760661.

When did STERILIZER WRAP (CAT#221831,2,3,4,5,6) receive FDA 510(k) clearance?

STERILIZER WRAP (CAT#221831,2,3,4,5,6) received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760661.

Who is the listed applicant for STERILIZER WRAP (CAT#221831,2,3,4,5,6)?

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

What is the FDA product code for STERILIZER WRAP (CAT#221831,2,3,4,5,6)?

The FDA product code for STERILIZER WRAP (CAT#221831,2,3,4,5,6) is FRG.

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Related Devices (Code: FRG)

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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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