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FDA 510(k)

GAS STERILIZATION POUCHES

K-Number: K821330 · 1982-06-07

ApplicantMedical Industries Packaging, Inc.
Decision Date1982-06-07
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GAS STERILIZATION POUCHES is the device name listed in this FDA 510(k) record. The listed applicant is Medical Industries Packaging, Inc.. It received FDA 510(k) clearance on 1982-06-07 under 510(k) number K821330. 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 GAS STERILIZATION POUCHES?

GAS STERILIZATION POUCHES is a medical device that received FDA 510(k) clearance on 1982-06-07. The listed applicant is Medical Industries Packaging, Inc.. The 510(k) number is K821330.

When did GAS STERILIZATION POUCHES receive FDA 510(k) clearance?

GAS STERILIZATION POUCHES received FDA 510(k) clearance on 1982-06-07, under 510(k) number K821330.

Who is the listed applicant for GAS STERILIZATION POUCHES?

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

What is the FDA product code for GAS STERILIZATION POUCHES?

The FDA product code for GAS STERILIZATION POUCHES is FRG.

Related Clinical Trials

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Other records listing Medical Industries Packaging, 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.

K832128SELF-SEAL STERILIZATION POUCHESK831165DUSTCOVERS/STERILITY MAINTENANCE COVERSK830961EASY BREATHER HEADER BAGSK821331MEDI-SEAL STERILIZATION POUCHES & TUBK821332DUSTCOVERS &/OR STERILITY MAINT. COVERS

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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