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FDA 510(k)

CATHETER, ARTERIAL LINE

K-Number: K790083 · 1979-01-25

ApplicantNamic
Decision Date1979-01-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHETER, ARTERIAL LINE is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1979-01-25 under 510(k) number K790083. 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 CATHETER, ARTERIAL LINE?

CATHETER, ARTERIAL LINE is a medical device that received FDA 510(k) clearance on 1979-01-25. The listed applicant is Namic. The 510(k) number is K790083.

When did CATHETER, ARTERIAL LINE receive FDA 510(k) clearance?

CATHETER, ARTERIAL LINE received FDA 510(k) clearance on 1979-01-25, under 510(k) number K790083.

Who is the listed applicant for CATHETER, ARTERIAL LINE?

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

What is the FDA product code for CATHETER, ARTERIAL LINE?

The FDA product code for CATHETER, ARTERIAL LINE is DQY.

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Other records listing Namic 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.

K953676BREEZE DIGITAL INFLATION DEVICEK951722PERCEPTOR COMPENSATOR MORSE MANIFOLDK921322MORSE ANESTHESIA MANIFOLDK822100HIGH PRESSURE CONTRAST INJECTION LINEK813549CONTINUOUS FLUSH DEVICEK790082ARTERIAL EXTENSION SET

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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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