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FDA 510(k)

ARTERIAL CANALIZATION DEVICE

K-Number: K820516 · 1982-04-15

ApplicantAlimed, Inc.
Decision Date1982-04-15
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIAL CANALIZATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Alimed, Inc.. It received FDA 510(k) clearance on 1982-04-15 under 510(k) number K820516. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL CANALIZATION DEVICE?

ARTERIAL CANALIZATION DEVICE is a medical device that received FDA 510(k) clearance on 1982-04-15. The listed applicant is Alimed, Inc.. The 510(k) number is K820516.

When did ARTERIAL CANALIZATION DEVICE receive FDA 510(k) clearance?

ARTERIAL CANALIZATION DEVICE received FDA 510(k) clearance on 1982-04-15, under 510(k) number K820516.

Who is the listed applicant for ARTERIAL CANALIZATION DEVICE?

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

What is the FDA product code for ARTERIAL CANALIZATION DEVICE?

The FDA product code for ARTERIAL CANALIZATION DEVICE is DQY.

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Other records listing Alimed, 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.

K963527UNIVERSAL ECONO-STRAP, QUALCRAFT UNIVERSAL STRAPSK963528ALIMED POSITIONING 7 SAFETY STRAPS (THREE TYPES), UNIVERSAL CR/MRI WIDE BODY STRAP, UNIVERSAL CT SCANNER STRAP (2 SIZES)K963526STRAP WEDGEK920487MINI VIBRATORK840156PROTECTA COAT SPONGESK822650SUPER DONUT

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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