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FDA 510(k)

POUCHES AND TUBING, MEDI-SEAL

K-Number: K781924 · 1978-11-22

ApplicantMedicare Industries, Inc.
Decision Date1978-11-22
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POUCHES AND TUBING, MEDI-SEAL is the device name listed in this FDA 510(k) record. The listed applicant is Medicare Industries, Inc.. It received FDA 510(k) clearance on 1978-11-22 under 510(k) number K781924. 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 POUCHES AND TUBING, MEDI-SEAL?

POUCHES AND TUBING, MEDI-SEAL is a medical device that received FDA 510(k) clearance on 1978-11-22. The listed applicant is Medicare Industries, Inc.. The 510(k) number is K781924.

When did POUCHES AND TUBING, MEDI-SEAL receive FDA 510(k) clearance?

POUCHES AND TUBING, MEDI-SEAL received FDA 510(k) clearance on 1978-11-22, under 510(k) number K781924.

Who is the listed applicant for POUCHES AND TUBING, MEDI-SEAL?

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

What is the FDA product code for POUCHES AND TUBING, MEDI-SEAL?

The FDA product code for POUCHES AND TUBING, MEDI-SEAL is FRG.

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Other records listing Medicare Industries, 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.

K894197LATEX EXAMINATION GLOVESK891865NIL (PATIENT EXAMINATION GLOVES - LATEX)K791434SPONGE COUNTER BAGSK781980RESPIRATORY THERAPY GAS POUCHK781981DECONTAMINATION ITEMS BAGK781925POUCHES, GAS STERILIZATION

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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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