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FDA 510(k)

CONTINUOUS FLUSH DEVICE/FDI

K-Number: K820202 · 1982-02-12

ApplicantLinton Biomed Corp.
Decision Date1982-02-12
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS FLUSH DEVICE/FDI is the device name listed in this FDA 510(k) record. The listed applicant is Linton Biomed Corp.. It received FDA 510(k) clearance on 1982-02-12 under 510(k) number K820202. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS FLUSH DEVICE/FDI?

CONTINUOUS FLUSH DEVICE/FDI is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is Linton Biomed Corp.. The 510(k) number is K820202.

When did CONTINUOUS FLUSH DEVICE/FDI receive FDA 510(k) clearance?

CONTINUOUS FLUSH DEVICE/FDI received FDA 510(k) clearance on 1982-02-12, under 510(k) number K820202.

Who is the listed applicant for CONTINUOUS FLUSH DEVICE/FDI?

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

What is the FDA product code for CONTINUOUS FLUSH DEVICE/FDI?

The FDA product code for CONTINUOUS FLUSH DEVICE/FDI is DRS.

Related Clinical Trials

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Other records listing Linton Biomed Corp. 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.

K841772HEPARIN CAP, INJECTION CAP MALE LUER-K831348FLUID ADMIN. SET AFS-1CK820201DISPOS. MONITORING SYS/LI ET ALK820203FLUID ADMINISTRATIVE SET, AFI

Related Devices (Code: DRS)

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.

K254074TruPressProcerus EnterprisesK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsEdwards Lifesciences, LLCK221782Meritrans ECO Reusable Pressure Transducer, Meritrans ECO DomesMerit Medical Pte. , Ltd.K172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K161408Compass Cast and MAPCenturion Medical Products Corporation

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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