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FDA 510(k)

CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS

K-Number: K871573 · 1987-09-16

ApplicantSpectramed, Inc.
Decision Date1987-09-16
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS is the device name listed in this FDA 510(k) record. The listed applicant is Spectramed, Inc.. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K871573. 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 CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS?

CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Spectramed, Inc.. The 510(k) number is K871573.

When did CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS receive FDA 510(k) clearance?

CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS received FDA 510(k) clearance on 1987-09-16, under 510(k) number K871573.

Who is the listed applicant for CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS?

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

What is the FDA product code for CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS?

The FDA product code for CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS is DQY.

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Other records listing Spectramed, 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.

K896122AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPEDK892941CCO SYSTEM MODEL SP1467,SP5567,SP6267K895323MODEL DT-BAL, BALANCE SAVERK894362MODEL DT-IUPC2 TRANSDUCER TIPPED DUAL LUMEN IUPK881857AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU.K885235SAFE-DRAW(TM) BLOOD SAMPLING RESERVOIR & ACCESS.

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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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