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FDA 510(k)

AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS

K-Number: K801331 · 1980-08-20

ApplicantAssociated Medical Products Co.
Decision Date1980-08-20
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Associated Medical Products Co.. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801331. 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 AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS?

AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Associated Medical Products Co.. The 510(k) number is K801331.

When did AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS receive FDA 510(k) clearance?

AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801331.

Who is the listed applicant for AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS?

The FDA 510(k) record lists Associated Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS?

The FDA product code for AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS is FRG.

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Other records listing Associated Medical Products Co. 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.

K932221NEUROLOGICAL OR CRANI TRAYS (PACKS)K932216C-SECTION, LABOR & DELIVERY TRAYS (PACKS)K930507CUSTOM ORTHOPAEDIC TRAYS (PACKS)K932217MAJOR, MINOR, BASIN TRAYS (PACKS)K932220LAP CHOLY TRAYS (PACKS)K932218CARDIAC CATH OR ANGIOGRAPHIC TRAYS

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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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